commit 326b99d43fdc9b210d2f5df79018ef03614ea684
Author: davidlagorce <david.lagorce@inserm.fr>
Date:   Tue Dec 9 16:49:50 2025 +0100

    DECEMBER 2025

diff --git a/Epidemiological data/Rare diseases natural history/nl_product9_ages.xml b/Epidemiological data/Rare diseases natural history/nl_product9_ages.xml
index 416cc22..d9a73ac 100755
--- a/Epidemiological data/Rare diseases natural history/nl_product9_ages.xml	
+++ b/Epidemiological data/Rare diseases natural history/nl_product9_ages.xml	
@@ -1,165888 +1,167901 @@
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-      <OrphaCode>812</OrphaCode>
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-      <Name lang="nl">Familiaal sick sinus-syndroom</Name>
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-      <OrphaCode>578</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=578</ExpertLink>
-      <Name lang="nl">Mucolipidose type IV</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="17629">
-      <OrphaCode>166286</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=166286</ExpertLink>
-      <Name lang="nl">Porokeratotische eccriene ostiale en dermale kanaalnaevus</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
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-      <OrphaCode>577</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=577</ExpertLink>
-      <Name lang="nl">Mucolipidose type III</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>166291</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=166291</ExpertLink>
-      <Name lang="nl">Dirofilariase</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>166308</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=166308</ExpertLink>
-      <Name lang="nl">Goedaardige infantiele focale epilepsie met pieken en golven in de middellijn tijdens de slaap</Name>
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-      <OrphaCode>2912</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2912</ExpertLink>
-      <Name lang="nl">Poliomyelitis</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <OrphaCode>796</OrphaCode>
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-      <Name lang="nl">Ziekte van Sandhoff</Name>
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-      <OrphaCode>166409</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=166409</ExpertLink>
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-      <OrphaCode>801</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=801</ExpertLink>
-      <Name lang="nl">Sclerodermie</Name>
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-      <Name lang="nl">Recessieve X-gebonden ichthyosis</Name>
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-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="17554">
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-          <Name lang="nl">Kindsheid</Name>
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-      <Name lang="nl">X-linked cerebral-cerebellar-coloboma syndrome</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="17567">
-      <OrphaCode>164726</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=164726</ExpertLink>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <OrphaCode>324</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324</ExpertLink>
-      <Name lang="nl">Ziekte van Fabry</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="17561">
-      <OrphaCode>163985</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=163985</ExpertLink>
-      <Name lang="nl">Hyperekplexie - epilepsie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="91">
-      <OrphaCode>778</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=778</ExpertLink>
-      <Name lang="nl">Syndroom van Rett</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
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-    <Disorder id="90">
-      <OrphaCode>72</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=72</ExpertLink>
-      <Name lang="nl">Syndroom van Angelman</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="102">
-      <OrphaCode>307</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=307</ExpertLink>
-      <Name lang="nl">Juveniele myoclonische epilepsie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="101">
-      <OrphaCode>1941</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1941</ExpertLink>
-      <Name lang="nl">Juveniele absence-epilepsie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="99">
-      <OrphaCode>892</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=892</ExpertLink>
-      <Name lang="nl">Ziekte van von Hippel-Lindau</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="97">
-      <OrphaCode>731</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=731</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve polycystische nierziekte</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="17568">
-      <OrphaCode>164736</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=164736</ExpertLink>
-      <Name lang="nl">Familiaal geavanceerde slaapfase-syndroom</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="110">
-      <OrphaCode>138</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=138</ExpertLink>
-      <Name lang="nl">CHARGE-syndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=558</ExpertLink>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Hermelijn-fenotype</Name>
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-      <Name lang="nl">Ernstige congenitale nemaline myopathie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=998</ExpertLink>
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-    <Disorder id="343">
-      <OrphaCode>1727</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1727</ExpertLink>
-      <Name lang="nl">22q11.2-duplicatiesyndroom</Name>
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-      <Name lang="nl">Cernunnos-XLF-deficiëntie</Name>
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-      <Name lang="nl">Trisomie 18p-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-    <Disorder id="339">
-      <OrphaCode>3380</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3380</ExpertLink>
-      <Name lang="nl">Trisomie 18-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-    <Disorder id="17810">
-      <OrphaCode>168984</OrphaCode>
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-      <Name lang="nl">CLAPO-syndroom</Name>
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-    <Disorder id="338">
-      <OrphaCode>1707</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1707</ExpertLink>
-      <Name lang="nl">Distale duplicatie 15q-syndroom</Name>
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-    <Disorder id="17811">
-      <OrphaCode>168999</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=168999</ExpertLink>
-      <Name lang="nl">Maligne melanoom van mucosa</Name>
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-      <Name lang="nl">Trisomie 13-syndroom</Name>
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-    <Disorder id="17820">
-      <OrphaCode>169100</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=169100</ExpertLink>
-      <Name lang="nl">Immuundeficiëntie door CD25-deficiëntie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=385</ExpertLink>
-      <Name lang="nl">Neurodegeneratie met ijzerstapeling in hersenen</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="3">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17830">
-      <OrphaCode>169157</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=169157</ExpertLink>
-      <Name lang="nl">Ernstige gecombineerde T- B+ immuundeficiëntie door CD45-deficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="353">
-      <OrphaCode>1947</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1947</ExpertLink>
-      <Name lang="nl">Progressieve epilepsie - intellectuele achterstand-syndroom, Fins type</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17827">
-      <OrphaCode>169147</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=169147</ExpertLink>
-      <Name lang="nl">Immuundeficiëntie door deficiëntie van een component van de klassieke route van het complementsysteem</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17826">
-      <OrphaCode>169142</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=169142</ExpertLink>
-      <Name lang="nl">Recidiverende infecties door specifieke granulaire deficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="355">
-      <OrphaCode>352</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=352</ExpertLink>
-      <Name lang="nl">Galactosemie</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="364">
-      <OrphaCode>596</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=596</ExpertLink>
-      <Name lang="nl">X-gebonden centronucleaire myopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="367">
-      <OrphaCode>610</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=610</ExpertLink>
-      <Name lang="nl">Spierdystrofie van Bethlem</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17833">
-      <OrphaCode>169186</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=169186</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve centronucleaire myopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="360">
-      <OrphaCode>464</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=464</ExpertLink>
-      <Name lang="nl">Incontinentia pigmenti</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="361">
-      <OrphaCode>3307</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3307</ExpertLink>
-      <Name lang="nl">Tetrasomie 18p-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17834">
-      <OrphaCode>169189</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=169189</ExpertLink>
-      <Name lang="nl">Autosomaal dominante centronucleaire myopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="5">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
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-    </Disorder>
-    <Disorder id="410">
-      <OrphaCode>44</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=44</ExpertLink>
-      <Name lang="nl">Neonatale adrenoleukodystrofie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="411">
-      <OrphaCode>56</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=56</ExpertLink>
-      <Name lang="nl">Alkaptonurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="408">
-      <OrphaCode>963</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=963</ExpertLink>
-      <Name lang="nl">Acromegalie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="5">
-        <AverageAgeOfOnset id="23536">
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-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23494">
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-        </TypeOfInheritance>
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-    <Disorder id="415">
-      <OrphaCode>1059</OrphaCode>
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-      <Name lang="nl">'Blue rubber bleb'-naevus</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      </DisorderGroup>
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-        <AverageAgeOfOnset id="23529">
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
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-    <Disorder id="412">
-      <OrphaCode>1006</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1006</ExpertLink>
-      <Name lang="nl">Alopecie met antilichaamdeficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-      </DisorderGroup>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
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-        <TypeOfInheritance id="23480">
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-    </Disorder>
-    <Disorder id="413">
-      <OrphaCode>1046</OrphaCode>
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-      <Name lang="nl">Letale hemolytische anemie - genitale anomalieën-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
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-      <OrphaCode>22</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=22</ExpertLink>
-      <Name lang="nl">Succinyl-semialdehyde-dehydrogenasedeficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="403">
-      <OrphaCode>29</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=29</ExpertLink>
-      <Name lang="nl">Mevalonacidurie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="407">
-      <OrphaCode>245</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=245</ExpertLink>
-      <Name lang="nl">Syndroom van Nager</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23438">
-          <Name lang="nl">Mitochondriale overerving</Name>
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-    <Disorder id="485">
-      <OrphaCode>1880</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1880</ExpertLink>
-      <Name lang="nl">Ebstein-malformatie van tricuspidalisklep</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="484">
-      <OrphaCode>255</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=255</ExpertLink>
-      <Name lang="nl">Doparesponsieve dystonie</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="487">
-      <OrphaCode>1915</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1915</ExpertLink>
-      <Name lang="nl">Foetaal alcoholsyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="486">
-      <OrphaCode>1885</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1885</ExpertLink>
-      <Name lang="nl">Geïsoleerde ectopia lentis</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="481">
-      <OrphaCode>1851</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1851</ExpertLink>
-      <Name lang="nl">Multicystische dysplastische nier</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="551">
-      <OrphaCode>660</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=660</ExpertLink>
-      <Name lang="nl">Omfalocele</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="548">
-      <OrphaCode>635</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=635</ExpertLink>
-      <Name lang="nl">Neuroblastoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2612</ExpertLink>
-      <Name lang="nl">Lineaire naevus sebaceus-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="546">
-      <OrphaCode>2635</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2635</ExpertLink>
-      <Name lang="nl">Metatropische dysplasie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2655</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2655</ExpertLink>
-      <Name lang="nl">Thanatofore dysplasie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="545">
-      <OrphaCode>606</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=606</ExpertLink>
-      <Name lang="nl">Proximale myotone myopathie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="558">
-      <OrphaCode>705</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=705</ExpertLink>
-      <Name lang="nl">Syndroom van Pendred</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="556">
-      <OrphaCode>2801</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2801</ExpertLink>
-      <Name lang="nl">Juveniele ziekte van Paget</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2785</ExpertLink>
-      <Name lang="nl">Osteopetrose met renale tubulaire acidose</Name>
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-      <Name lang="nl">Prune belly-syndroom</Name>
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-      <Name lang="nl">Geïsoleerde Pierre Robin sequentie</Name>
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-    <Disorder id="575">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=290</ExpertLink>
-      <Name lang="nl">Congenitaal rubellasyndroom</Name>
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-    <Disorder id="574">
-      <OrphaCode>3071</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3071</ExpertLink>
-      <Name lang="nl">Syndroom van Costello</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>763</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=763</ExpertLink>
-      <Name lang="nl">Pycnodysostose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="570">
-      <OrphaCode>2983</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2983</ExpertLink>
-      <Name lang="nl">Geslachtsontwikkelingsstoornis - intellectuele achterstand-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="516">
-      <OrphaCode>2301</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2301</ExpertLink>
-      <Name lang="nl">Congenitaal kortedarmsyndroom</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="517">
-      <OrphaCode>469</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=469</ExpertLink>
-      <Name lang="nl">Erfelijke fructose-intolerantie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>2308</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2308</ExpertLink>
-      <Name lang="nl">Syndroom van Jacobsen</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2318</ExpertLink>
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-          <Name lang="nl">Neonataal</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-      <Name lang="nl">Gemengde kiemceltumor</Name>
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-      <Name lang="nl">Maligne tumor van eileider</Name>
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-      <Name lang="nl">Folliculotrope mycosis fungoides</Name>
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-      <OrphaCode>178509</OrphaCode>
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-      <OrphaCode>611</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=611</ExpertLink>
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-      <OrphaCode>2882</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2882</ExpertLink>
-      <Name lang="nl">Sitosterolemie</Name>
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-    <Disorder id="754">
-      <OrphaCode>810</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=810</ExpertLink>
-      <Name lang="nl">Shigellose</Name>
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-    <Disorder id="755">
-      <OrphaCode>3165</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3165</ExpertLink>
-      <Name lang="nl">Eosinofiele fasciitis</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="752">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2420</ExpertLink>
-      <Name lang="nl">Primair pulmonaal lymfoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="753">
-      <OrphaCode>727</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=727</ExpertLink>
-      <Name lang="nl">Microscopische polyangiitis</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="759">
-      <OrphaCode>900</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=900</ExpertLink>
-      <Name lang="nl">Granulomatose met polyangiitis</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="757">
-      <OrphaCode>863</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=863</ExpertLink>
-      <Name lang="nl">Trichinellose</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="17928">
-      <OrphaCode>171695</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=171695</ExpertLink>
-      <Name lang="nl">Parkinson-piramidaal syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="713">
-      <OrphaCode>134</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=134</ExpertLink>
-      <Name lang="nl">Bèta-ketothiolasedeficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="17929">
-      <OrphaCode>171700</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=171700</ExpertLink>
-      <Name lang="nl">Diffuse panbronchiolitis</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-      <OrphaCode>171703</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=171703</ExpertLink>
-      <Name lang="nl">Microcefalie - polymicrogyrie - agenesie van corpus callosum-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>171706</OrphaCode>
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-      <Name lang="nl">Mannelijke onvruchtbaarheid als gevolg van globozoöspermie</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="17945">
-      <OrphaCode>171863</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=171863</ExpertLink>
-      <Name lang="nl">Autosomaal dominante spastische paraplegie type 42</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="17947">
-      <OrphaCode>171871</OrphaCode>
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-      <Name lang="nl">Renaal pseudohypoaldosteronisme type 1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="730">
-      <OrphaCode>322</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=322</ExpertLink>
-      <Name lang="nl">Exstrofie - epispadie-complex</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-    <Disorder id="17946">
-      <OrphaCode>171866</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=171866</ExpertLink>
-      <Name lang="nl">Spondylo-epimetafysaire dysplasie, aggrecan-type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="731">
-      <OrphaCode>2368</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2368</ExpertLink>
-      <Name lang="nl">Gastroschisis</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="17949">
-      <OrphaCode>171881</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=171881</ExpertLink>
-      <Name lang="nl">Cap-myopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="732">
-      <OrphaCode>2512</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2512</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve primaire microcefalie</Name>
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-        <Name lang="nl">Etiologisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="17948">
-      <OrphaCode>171876</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=171876</ExpertLink>
-      <Name lang="nl">Gegeneraliseerd pseudohypoaldosteronisme type 1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="734">
-      <OrphaCode>795</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=795</ExpertLink>
-      <Name lang="nl">Zeldzame vorm van salmonellose</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=797</ExpertLink>
-      <Name lang="nl">Sarcoïdose</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-        <TypeOfInheritance id="23424">
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-      <OrphaCode>92</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=92</ExpertLink>
-      <Name lang="nl">Juveniele idiopathische artritis</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <Name lang="nl">6q16-microdeletiesyndroom</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <AverageAgeOfOnset id="23529">
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-      <Name lang="nl">Geïsoleerde autosomaal dominante hypomagnesiëmie, Glaudemans-type</Name>
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-      <Name lang="nl">Congenitaal lobair emfyseem</Name>
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-      <Name lang="nl">Endocrien-cerebro-osteodysplasie-syndroom</Name>
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-      <OrphaCode>199329</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=199329</ExpertLink>
-      <Name lang="nl">Congenitale myopathie, Paradas-type</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="803">
-      <OrphaCode>2665</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2665</ExpertLink>
-      <Name lang="nl">Congenitaal mesoblastisch nefroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3463</ExpertLink>
-      <Name lang="nl">Syndroom van Wolfram</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=199642</ExpertLink>
-      <Name lang="nl">Geïsoleerde congenitale microcefalie</Name>
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-      <Name lang="nl">Veteranenziekte</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=267</ExpertLink>
-      <Name lang="nl">Calpaïne-3-gerelateerde limb-girdle-spierdystrofie R1</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="871">
-      <OrphaCode>1329</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1329</ExpertLink>
-      <Name lang="nl">Totaal atrioventriculair septumdefect</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="872">
-      <OrphaCode>582</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=582</ExpertLink>
-      <Name lang="nl">Mucopolysacharidose type 4</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="873">
-      <OrphaCode>2137</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2137</ExpertLink>
-      <Name lang="nl">Auto-immune hepatitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="874">
-      <OrphaCode>186</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=186</ExpertLink>
-      <Name lang="nl">Primaire biliaire cholangitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="876">
-      <OrphaCode>397</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=397</ExpertLink>
-      <Name lang="nl">Reuscelarteriitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="877">
-      <OrphaCode>2932</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2932</ExpertLink>
-      <Name lang="nl">Chronische inflammatoire demyeliniserende polyneuropathie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="878">
-      <OrphaCode>2398</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2398</ExpertLink>
-      <Name lang="nl">Multipele symmetrische lipomatose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23438">
-          <Name lang="nl">Mitochondriale overerving</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="879">
-      <OrphaCode>1656</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1656</ExpertLink>
-      <Name lang="nl">Dermatitis herpetiformis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="849">
-      <OrphaCode>3198</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3198</ExpertLink>
-      <Name lang="nl">Stiff person-spectrumstoornis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="5">
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="848">
-      <OrphaCode>2929</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2929</ExpertLink>
-      <Name lang="nl">Juveniele polyposis-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="854">
-      <OrphaCode>131</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=131</ExpertLink>
-      <Name lang="nl">Syndroom van Budd-Chiari</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="853">
-      <OrphaCode>646</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=646</ExpertLink>
-      <Name lang="nl">Ziekte van Niemann-Pick type C</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="852">
-      <OrphaCode>654</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=654</ExpertLink>
-      <Name lang="nl">Nefroblastoom</Name>
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-    <Disorder id="859">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1489</ExpertLink>
-      <Name lang="nl">Kinkhoest</Name>
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-    <Disorder id="858">
-      <OrphaCode>2764</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2764</ExpertLink>
-      <Name lang="nl">Osteochondritis dissecans</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="857">
-      <OrphaCode>2587</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2587</ExpertLink>
-      <Name lang="nl">Deficiëntie van myeloperoxidase</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="863">
-      <OrphaCode>3389</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3389</ExpertLink>
-      <Name lang="nl">Tuberculose</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-    <Disorder id="862">
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-      <Name lang="nl">Difterie</Name>
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-      <Name lang="nl">Botulisme</Name>
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-    <Disorder id="860">
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-      <Name lang="nl">Pityriasis rubra pilaris</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1078">
-      <OrphaCode>1444</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1444</ExpertLink>
-      <Name lang="nl">Ringchromosoom 20-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1077">
-      <OrphaCode>1439</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1439</ExpertLink>
-      <Name lang="nl">Ringchromosoom 12-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1076">
-      <OrphaCode>1438</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1438</ExpertLink>
-      <Name lang="nl">Ringchromosoom 10-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1222">
-      <OrphaCode>624</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=624</ExpertLink>
-      <Name lang="nl">Familiale multipele naevi flammei</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1228">
-      <OrphaCode>3306</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3306</ExpertLink>
-      <Name lang="nl">Inversie/duplicatie van chromosoom 15-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1231">
-      <OrphaCode>3375</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3375</ExpertLink>
-      <Name lang="nl">Trisomie X-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1230">
-      <OrphaCode>3310</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3310</ExpertLink>
-      <Name lang="nl">Tetrasomie 9p-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1225">
-      <OrphaCode>3000</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3000</ExpertLink>
-      <Name lang="nl">Familiale vroegtijdige puberteit beperkt tot mannen</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="1227">
-      <OrphaCode>3305</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3305</ExpertLink>
-      <Name lang="nl">Tetraploïdiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1226">
-      <OrphaCode>3176</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3176</ExpertLink>
-      <Name lang="nl">Spina bifida - hypospadie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1236">
-      <OrphaCode>1708</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1708</ExpertLink>
-      <Name lang="nl">Mozaïektrisomie 16-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
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-      </TypeOfInheritanceList>
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-    <Disorder id="1237">
-      <OrphaCode>1711</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1711</ExpertLink>
-      <Name lang="nl">Mozaïektrisomie 17-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-    <Disorder id="1232">
-      <OrphaCode>3376</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3376</ExpertLink>
-      <Name lang="nl">Triploïdiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="1233">
-      <OrphaCode>1692</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1692</ExpertLink>
-      <Name lang="nl">Mozaïektrisomie 1-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      </TypeOfInheritanceList>
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-    <Disorder id="1234">
-      <OrphaCode>1698</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1698</ExpertLink>
-      <Name lang="nl">Mozaïektrisomie 12-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-    <Disorder id="1235">
-      <OrphaCode>1706</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1706</ExpertLink>
-      <Name lang="nl">Mozaïektrisomie 15-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      </TypeOfInheritanceList>
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-    <Disorder id="1244">
-      <OrphaCode>916</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=916</ExpertLink>
-      <Name lang="nl">Syndroom van Aase-Smith</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1247">
-      <OrphaCode>920</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=920</ExpertLink>
-      <Name lang="nl">Ablefaron - macrostomie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="1241">
-      <OrphaCode>1445</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1445</ExpertLink>
-      <Name lang="nl">Ringchromosoom 21-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      </TypeOfInheritanceList>
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-      <OrphaCode>7</OrphaCode>
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-      <Name lang="nl">3C-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1255">
-      <OrphaCode>931</OrphaCode>
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-      <Name lang="nl">Geïsoleerde acheiropodie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="1254">
-      <OrphaCode>929</OrphaCode>
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-      <Name lang="nl">Achalasie - microcefalie-syndroom</Name>
-      <DisorderType id="21401">
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="1253">
-      <OrphaCode>869</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=869</ExpertLink>
-      <Name lang="nl">Triple A-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1251">
-      <OrphaCode>2297</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2297</ExpertLink>
-      <Name lang="nl">Insulineresistentiesyndroom type A</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1249">
-      <OrphaCode>922</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=922</ExpertLink>
-      <Name lang="nl">Familiale nasale acilie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1248">
-      <OrphaCode>921</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=921</ExpertLink>
-      <Name lang="nl">Syndroom van Abruzzo-Erickson</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="1263">
-      <OrphaCode>27</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=27</ExpertLink>
-      <Name lang="nl">Vitamine B12-resistente methylmalonacidemie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="1260">
-      <OrphaCode>939</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=939</ExpertLink>
-      <Name lang="nl">3-hydroxyisoboterzuuracidurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1259">
-      <OrphaCode>31</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=31</ExpertLink>
-      <Name lang="nl">Oxoglutaaracidurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="1258">
-      <OrphaCode>935</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=935</ExpertLink>
-      <Name lang="nl">Skeletdysplasie met korte ledematen en met ernstige gecombineerde immuundeficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1256">
-      <OrphaCode>932</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=932</ExpertLink>
-      <Name lang="nl">Achondrogenesie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="1268">
-      <OrphaCode>37</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=37</ExpertLink>
-      <Name lang="nl">Acrodermatitis enteropathica</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="1269">
-      <OrphaCode>950</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=950</ExpertLink>
-      <Name lang="nl">Acrodysostose</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
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-    <Disorder id="1267">
-      <OrphaCode>949</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=949</ExpertLink>
-      <Name lang="nl">Acrocraniofaciale dysostose</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    </Disorder>
-    <Disorder id="1264">
-      <OrphaCode>945</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=945</ExpertLink>
-      <Name lang="nl">Acalvaria</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1278">
-      <OrphaCode>957</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=957</ExpertLink>
-      <Name lang="nl">Acropectorovertebrale dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1279">
-      <OrphaCode>958</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=958</ExpertLink>
-      <Name lang="nl">Acro-renaal-mandibulair syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
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-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1276">
-      <OrphaCode>955</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=955</ExpertLink>
-      <Name lang="nl">Syndroom van Hajdu-Cheney</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="1272">
-      <OrphaCode>952</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=952</ExpertLink>
-      <Name lang="nl">Acrofaciale dysostose, Weyers-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="1153">
-      <OrphaCode>1702</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1702</ExpertLink>
-      <Name lang="nl">Niet-distale duplicatie 13q-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-    <Disorder id="1154">
-      <OrphaCode>1703</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1703</ExpertLink>
-      <Name lang="nl">Mozaïektrisomie 14-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-    <Disorder id="1156">
-      <OrphaCode>1705</OrphaCode>
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-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-        <AverageAgeOfOnset id="23522">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1178">
-      <OrphaCode>1742</OrphaCode>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="1352">
-      <OrphaCode>1053</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1053</ExpertLink>
-      <Name lang="nl">Aneurysmale malformatie van vena Galeni</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>1055</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1055</ExpertLink>
-      <Name lang="nl">Congenitaal linkerventrikelaneurysma</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1351">
-      <OrphaCode>1052</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1052</ExpertLink>
-      <Name lang="nl">Variabele aneuploïdie-mozaïek-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1346">
-      <OrphaCode>1040</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1040</ExpertLink>
-      <Name lang="nl">Metafysaire anadysplasie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1347">
-      <OrphaCode>1041</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1041</ExpertLink>
-      <Name lang="nl">Hydrops foetalis</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <OrphaCode>1037</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1037</ExpertLink>
-      <Name lang="nl">Arthrogryposis multiplex congenita</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1405">
-      <OrphaCode>1126</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1126</ExpertLink>
-      <Name lang="nl">Aprosencefalie cerebellaire dysgenesie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <OrphaCode>1125</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1125</ExpertLink>
-      <Name lang="nl">Oculomotorische apraxie, Cogan-type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1401">
-      <OrphaCode>1121</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1121</ExpertLink>
-      <Name lang="nl">Radiale deficiëntie - tibiale hypoplasie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-    <Disorder id="1400">
-      <OrphaCode>1120</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1120</ExpertLink>
-      <Name lang="nl">Longagenesie - hartdefect - duimanomalieën-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-    <Disorder id="1402">
-      <OrphaCode>1122</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1122</ExpertLink>
-      <Name lang="nl">Hypoplasie van ulna - gespleten voet-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1397">
-      <OrphaCode>1116</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1116</ExpertLink>
-      <Name lang="nl">Aplasia cutis congenita - intestinale lymfangiëctasie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>1118</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1118</ExpertLink>
-      <Name lang="nl">Fibulaire aplasie - ectrodactylie-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Agnathie - holoprosencefalie - situs inversus-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1304">
-      <OrphaCode>989</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=989</ExpertLink>
-      <Name lang="nl">Hypoglossie - hypodactylie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    </Disorder>
-    <Disorder id="1310">
-      <OrphaCode>994</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=994</ExpertLink>
-      <Name lang="nl">Foetale akinesie - deformatie-sequentie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1309">
-      <OrphaCode>51</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=51</ExpertLink>
-      <Name lang="nl">Syndroom van Aicardi-Goutières</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="1299">
-      <OrphaCode>981</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=981</ExpertLink>
-      <Name lang="nl">Afwezigheid van arteria carotis interna</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="1297">
-      <OrphaCode>978</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=978</ExpertLink>
-      <Name lang="nl">ADULT-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    </Disorder>
-    <Disorder id="1296">
-      <OrphaCode>977</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=977</ExpertLink>
-      <Name lang="nl">Adrenomyodystrofie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="1303">
-      <OrphaCode>988</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=988</ExpertLink>
-      <Name lang="nl">Hemimelie van tibia - polysyndactylie - trifalangeale duim-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1300">
-      <OrphaCode>983</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=983</ExpertLink>
-      <Name lang="nl">Testiculaire regressie-syndroom</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1290">
-      <OrphaCode>970</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=970</ExpertLink>
-      <Name lang="nl">Erfelijke sensorische en autonome neuropathie type 2</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1291">
-      <OrphaCode>971</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=971</ExpertLink>
-      <Name lang="nl">Acrorenaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1288">
-      <OrphaCode>40</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=40</ExpertLink>
-      <Name lang="nl">Acromesomele dysplasie, Maroteaux-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1289">
-      <OrphaCode>969</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=969</ExpertLink>
-      <Name lang="nl">Acromicrische dysplasie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Syndroom van Adams-Oliver</Name>
-      <DisorderType id="21401">
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
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-      <OrphaCode>972</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=972</ExpertLink>
-      <Name lang="nl">Erfelijke continue spiervezelactiviteit</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
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-        <AverageAgeOfOnset id="23522">
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-    <Disorder id="1293">
-      <OrphaCode>973</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=973</ExpertLink>
-      <Name lang="nl">Geïsoleerde afwezigheid/hypoplasie van vingers exclusief duim, unilateraal</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1280">
-      <OrphaCode>959</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=959</ExpertLink>
-      <Name lang="nl">Acro-renaal-oculair syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="1287">
-      <OrphaCode>968</OrphaCode>
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-        <AverageAgeOfOnset id="23515">
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-    <Disorder id="16888">
-      <OrphaCode>139411</OrphaCode>
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-        <AverageAgeOfOnset id="23536">
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-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="1339">
-      <OrphaCode>1031</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1031</ExpertLink>
-      <Name lang="nl">Tandglazuur - nieren-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="16892">
-      <OrphaCode>139423</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139423</ExpertLink>
-      <Name lang="nl">Idiopathische acute transversale myelitis</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="16893">
-      <OrphaCode>139426</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139426</ExpertLink>
-      <Name lang="nl">Periorale myoclonus met absences</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="16894">
-      <OrphaCode>139431</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139431</ExpertLink>
-      <Name lang="nl">Epilepsie met myoclonie van ooglid</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="1342">
-      <OrphaCode>1035</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1035</ExpertLink>
-      <Name lang="nl">Bèta-mercaptolactaat-cysteïne-disulfidurie</Name>
-      <DisorderType id="21408">
-        <Name lang="nl">Biologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="16895">
-      <OrphaCode>139436</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139436</ExpertLink>
-      <Name lang="nl">Multicentrische reticulohistiocytose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1329">
-      <OrphaCode>1021</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1021</ExpertLink>
-      <Name lang="nl">Amaurosis - hypertrichose-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1328">
-      <OrphaCode>64</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64</ExpertLink>
-      <Name lang="nl">Syndroom van Alström</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="5">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1331">
-      <OrphaCode>1023</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1023</ExpertLink>
-      <Name lang="nl">Congenitale gegeneraliseerde hypertrichose, Ambras-type</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="16882">
-      <OrphaCode>139390</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139390</ExpertLink>
-      <Name lang="nl">Niet-syndromale craniosynostose</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="16884">
-      <OrphaCode>139396</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139396</ExpertLink>
-      <Name lang="nl">X-gebonden cerebrale adrenoleukodystrofie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="16885">
-      <OrphaCode>139399</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139399</ExpertLink>
-      <Name lang="nl">Adrenomyeloneuropathie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="16886">
-      <OrphaCode>139402</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139402</ExpertLink>
-      <Name lang="nl">Reactie op medicatie met eosinofilie en systemische symptomen</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
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-      <OrphaCode>139406</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139406</ExpertLink>
-      <Name lang="nl">Encefalopathie door deficiëntie van prosaposine</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="1320">
-      <OrphaCode>1008</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1008</ExpertLink>
-      <Name lang="nl">Alopecie - epilepsie - pyorree - intellectuele achterstand-syndroom</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-      <OrphaCode>701</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=701</ExpertLink>
-      <Name lang="nl">Alopecia universalis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1010</ExpertLink>
-      <Name lang="nl">Autosomaal dominante palmoplantaire keratodermie en congenitale alopecie</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>1014</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1014</ExpertLink>
-      <Name lang="nl">Alopecie - intellectuele achterstand - hypergonadotroop hypogonadisme-syndroom</Name>
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-        <AverageAgeOfOnset id="23515">
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-        <TypeOfInheritance id="23480">
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-      <Name lang="nl">2q37-microdeletiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Syndroom van Allan-Herndon-Dudley</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Defecten van scalp - postaxiale polydactylie-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Blefaronasofaciale malformatie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">X-gebonden dominant</Name>
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-    <Disorder id="1490">
-      <OrphaCode>1248</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1248</ExpertLink>
-      <Name lang="nl">Maxillonasale dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-    <Disorder id="1502">
-      <OrphaCode>127</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=127</ExpertLink>
-      <Name lang="nl">Syndroom van Borjeson-Forssman-Lehmann</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1503">
-      <OrphaCode>1264</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1264</ExpertLink>
-      <Name lang="nl">Tricho-retino-dento-digitaal syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1500">
-      <OrphaCode>1262</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1262</ExpertLink>
-      <Name lang="nl">Syndroom van Böök</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="1501">
-      <OrphaCode>1263</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1263</ExpertLink>
-      <Name lang="nl">Boemerang-dysplasie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1498">
-      <OrphaCode>1259</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1259</ExpertLink>
-      <Name lang="nl">Blefaroptose - myopie - ectopia lentis-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="1499">
-      <OrphaCode>1261</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1261</ExpertLink>
-      <Name lang="nl">Syndroom van Bonnemann-Meinecke-Reich</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1478">
-      <OrphaCode>1234</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1234</ExpertLink>
-      <Name lang="nl">Syndroom van Bartsocas-Papas</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1476">
-      <OrphaCode>1231</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1231</ExpertLink>
-      <Name lang="nl">Syndroom van Barber-Say</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1229</ExpertLink>
-      <Name lang="nl">Congenitaal intra-uterien infectieachtig syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <OrphaCode>109</OrphaCode>
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-      <Name lang="nl">Syndroom van Bannayan-Riley-Ruvalcaba</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <OrphaCode>137608</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137608</ExpertLink>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1299</ExpertLink>
-      <Name lang="nl">Branchioskeletogenitaal syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <OrphaCode>1300</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1300</ExpertLink>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="16702">
-      <OrphaCode>137667</OrphaCode>
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-      <Name lang="nl">Capillaire malformatie-arterioveneuze malformatie</Name>
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-      <OrphaCode>1295</OrphaCode>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137631</ExpertLink>
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-      <Name lang="nl">Syndroom van Lambert</Name>
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-      <OrphaCode>137639</OrphaCode>
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-      <Name lang="nl">Syndroom van Frank-Ter Haar</Name>
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-      <Name lang="nl">Autosomaal recessieve cerebelloparenchymale aandoening type 3</Name>
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-      <Name lang="nl">Goedaardig paroxysmaal tonisch omhoogdraaien van ogen in de kindertijd met ataxie</Name>
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-      <Name lang="nl">Motorneuronziekte van Madras</Name>
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-    <Disorder id="1444">
-      <OrphaCode>1187</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1187</ExpertLink>
-      <Name lang="nl">Letale ataxie met doofheid en opticusatrofie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1447">
-      <OrphaCode>1190</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1190</ExpertLink>
-      <Name lang="nl">Atelosteogenese type I</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="16742">
-      <OrphaCode>137908</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137908</ExpertLink>
-      <Name lang="nl">Hypotonie met melkzuuracidemie en hyperammoniëmie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="16744">
-      <OrphaCode>137914</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137914</ExpertLink>
-      <Name lang="nl">Choane atresie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1449">
-      <OrphaCode>1193</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1193</ExpertLink>
-      <Name lang="nl">Syndroom van Atkin-Flaitz</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="16745">
-      <OrphaCode>137917</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137917</ExpertLink>
-      <Name lang="nl">Choane atresie, unilaterale</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1451">
-      <OrphaCode>1200</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1200</ExpertLink>
-      <Name lang="nl">Syndroom van Burn-McKeown</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="16746">
-      <OrphaCode>137920</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137920</ExpertLink>
-      <Name lang="nl">Choane atresie, bilaterale</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1450">
-      <OrphaCode>1198</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1198</ExpertLink>
-      <Name lang="nl">Colonatresie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="16748">
-      <OrphaCode>137926</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137926</ExpertLink>
-      <Name lang="nl">Primair laryngeaal lymfangioom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1452">
-      <OrphaCode>1203</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1203</ExpertLink>
-      <Name lang="nl">Duodenumatresie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1455">
-      <OrphaCode>1208</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1208</ExpertLink>
-      <Name lang="nl">Pulmonale atresie - intact ventrikelseptum-syndroom</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="16750">
-      <OrphaCode>137932</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137932</ExpertLink>
-      <Name lang="nl">Congenitale laryngeale paralyse</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="16751">
-      <OrphaCode>137935</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=137935</ExpertLink>
-      <Name lang="nl">Laryngotracheaal angioom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1642">
-      <OrphaCode>1449</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1449</ExpertLink>
-      <Name lang="nl">Ringchromosoom 7-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17067">
-      <OrphaCode>141242</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141242</ExpertLink>
-      <Name lang="nl">Paramediane nasale spleet</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1643">
-      <OrphaCode>1453</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1453</ExpertLink>
-      <Name lang="nl">Cleidorhizomeel syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="1640">
-      <OrphaCode>1440</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1440</ExpertLink>
-      <Name lang="nl">Ringchromosoom 14-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    </Disorder>
-    <Disorder id="17065">
-      <OrphaCode>141234</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141234</ExpertLink>
-      <Name lang="nl">Mediane aangezichtsspleet</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1641">
-      <OrphaCode>1443</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1443</ExpertLink>
-      <Name lang="nl">Ringchromosoom 19-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="17071">
-      <OrphaCode>141261</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141261</ExpertLink>
-      <Name lang="nl">Aangezichtsspleet Tessier nummer 5</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      </TypeOfInheritanceList>
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-    <Disorder id="17070">
-      <OrphaCode>141258</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141258</ExpertLink>
-      <Name lang="nl">Aangezichtsspleet Tessier nummer 4</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1647">
-      <OrphaCode>1458</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1458</ExpertLink>
-      <Name lang="nl">CODAS-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="17069">
-      <OrphaCode>141253</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141253</ExpertLink>
-      <Name lang="nl">Schuine aangezichtsspleet</Name>
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-    <Disorder id="1644">
-      <OrphaCode>1454</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1454</ExpertLink>
-      <Name lang="nl">Syndroom van Joubert met hepatisch defect</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1645">
-      <OrphaCode>190</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=190</ExpertLink>
-      <Name lang="nl">Ziekte van Coats</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="17059">
-      <OrphaCode>141199</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141199</ExpertLink>
-      <Name lang="nl">Cerebrofaciaal arterioveneus metamerisch syndroom type 3</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1634">
-      <OrphaCode>1429</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1429</ExpertLink>
-      <Name lang="nl">Goedaardige erfelijke chorea</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="17058">
-      <OrphaCode>141194</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141194</ExpertLink>
-      <Name lang="nl">Cerebrofaciaal arterioveneus metamerisch syndroom type 1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="1632">
-      <OrphaCode>1426</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1426</ExpertLink>
-      <Name lang="nl">Dysplasie van Greenberg</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="17056">
-      <OrphaCode>141184</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141184</ExpertLink>
-      <Name lang="nl">Snel involuerend congenitaal hemangioom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1633">
-      <OrphaCode>1427</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1427</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve otospondylomega-epifysaire dysplasie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1638">
-      <OrphaCode>1435</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1435</ExpertLink>
-      <Name lang="nl">Xq21-microdeletiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1639">
-      <OrphaCode>1436</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1436</ExpertLink>
-      <Name lang="nl">X-gebonden skeletdysplasie - intellectuele achterstand-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="17062">
-      <OrphaCode>141214</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141214</ExpertLink>
-      <Name lang="nl">Geïsoleerde congenitale syngnathie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="17061">
-      <OrphaCode>141209</OrphaCode>
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-      <Name lang="nl">Diffuse lymfatische malformatie</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-      <Name lang="nl">Choroïdale atrofie - alopecie-syndroom</Name>
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-      <OrphaCode>1484</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1484</ExpertLink>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141333</ExpertLink>
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-        <TypeOfInheritance id="23480">
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-    <Disorder id="1663">
-      <OrphaCode>1490</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1490</ExpertLink>
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-      <Name lang="nl">Aangezichtsspleet Tessier nummer 7</Name>
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-    <Disorder id="17073">
-      <OrphaCode>141269</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141269</ExpertLink>
-      <Name lang="nl">Laterale aangezichtsspleet</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1654">
-      <OrphaCode>1471</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1471</ExpertLink>
-      <Name lang="nl">Maculacoloboom - brachydactylie type B-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17076">
-      <OrphaCode>141288</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141288</ExpertLink>
-      <Name lang="nl">Mediane cervicale splijting</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17077">
-      <OrphaCode>141291</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141291</ExpertLink>
-      <Name lang="nl">Schisis van lip en alveole</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17033">
-      <OrphaCode>141091</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141091</ExpertLink>
-      <Name lang="nl">Polyrhinie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17032">
-      <OrphaCode>141083</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141083</ExpertLink>
-      <Name lang="nl">Cyste van ductus nasolacrimalis</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1610">
-      <OrphaCode>1410</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1410</ExpertLink>
-      <Name lang="nl">Onkambaar haar-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17035">
-      <OrphaCode>141099</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141099</ExpertLink>
-      <Name lang="nl">Proboscis lateralis</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17034">
-      <OrphaCode>141096</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141096</ExpertLink>
-      <Name lang="nl">Surnumeraire neusvleugel</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1612">
-      <OrphaCode>1412</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1412</ExpertLink>
-      <Name lang="nl">Tarsale-carpale coalitie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1614">
-      <OrphaCode>1416</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1416</ExpertLink>
-      <Name lang="nl">Familiale depositie van calciumpyrofosfaat</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17038">
-      <OrphaCode>141112</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141112</ExpertLink>
-      <Name lang="nl">Nasale gliale heterotopie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1600">
-      <OrphaCode>1394</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1394</ExpertLink>
-      <Name lang="nl">Cerebrofaciothoracale dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1604">
-      <OrphaCode>1397</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1397</ExpertLink>
-      <Name lang="nl">Hydrocefalie - cerebellaire agenesie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1605">
-      <OrphaCode>1398</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1398</ExpertLink>
-      <Name lang="nl">Geïsoleerde cerebellaire agenesie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1606">
-      <OrphaCode>1399</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1399</ExpertLink>
-      <Name lang="nl">Syndroom van Richards-Rundle</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17031">
-      <OrphaCode>141077</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141077</ExpertLink>
-      <Name lang="nl">Epignathus</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1607">
-      <OrphaCode>1401</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1401</ExpertLink>
-      <Name lang="nl">CHAND-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17030">
-      <OrphaCode>141074</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141074</ExpertLink>
-      <Name lang="nl">Aplasie/hypoplasie van uitwendige gehoorgang</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17048">
-      <OrphaCode>141152</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141152</ExpertLink>
-      <Name lang="nl">Geïsoleerde congenitale hypoglossie/aglossie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1624">
-      <OrphaCode>174</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=174</ExpertLink>
-      <Name lang="nl">Metafysaire chondrodysplasie, Schmid-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17051">
-      <OrphaCode>141163</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141163</ExpertLink>
-      <Name lang="nl">Glossopalatinale ankylose</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17052">
-      <OrphaCode>141168</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141168</ExpertLink>
-      <Name lang="nl">Frontonasale arterioveneuze malformatie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17053">
-      <OrphaCode>141171</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141171</ExpertLink>
-      <Name lang="nl">Maxillaire arterioveneuze malformatie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="1631">
-      <OrphaCode>1425</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1425</ExpertLink>
-      <Name lang="nl">Syndroom van Desbuquois</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="17054">
-      <OrphaCode>141174</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141174</ExpertLink>
-      <Name lang="nl">Mandibulaire arterioveneuze malformatie</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="17055">
-      <OrphaCode>141179</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141179</ExpertLink>
-      <Name lang="nl">Niet-involuerend congenitaal hemangioom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="17040">
-      <OrphaCode>141118</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141118</ExpertLink>
-      <Name lang="nl">Nasale encefalocele</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="17041">
-      <OrphaCode>141121</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141121</ExpertLink>
-      <Name lang="nl">Congenitale subglottisstenose</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
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-          <Name lang="nl">Neonataal</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="17043">
-      <OrphaCode>141127</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141127</ExpertLink>
-      <Name lang="nl">Congenitale tracheale stenose</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="17044">
-      <OrphaCode>141132</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141132</ExpertLink>
-      <Name lang="nl">Oculo-auriculo-vertebraal spectrum</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="17046">
-      <OrphaCode>141145</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141145</ExpertLink>
-      <Name lang="nl">Hemifaciale hyperplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="17047">
-      <OrphaCode>141148</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=141148</ExpertLink>
-      <Name lang="nl">Hemifaciale myohyperplasie</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="17135">
-      <OrphaCode>156728</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=156728</ExpertLink>
-      <Name lang="nl">Spondylo-epimetafysaire dysplasie, matriline 3-type</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1582">
-      <OrphaCode>1375</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1375</ExpertLink>
-      <Name lang="nl">Cataract - hypertrichose - intellectuele achterstand-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1580">
-      <OrphaCode>163</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=163</ExpertLink>
-      <Name lang="nl">Hereditaire hyperferritinemie - cataract-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="1579">
-      <OrphaCode>1373</OrphaCode>
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-      <Name lang="nl">Cataract - afwijkend oraal frenulum - groeiachterstand-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="1575">
-      <OrphaCode>1368</OrphaCode>
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-      <Name lang="nl">Carnosinasedeficiëntie</Name>
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-      <Name lang="nl">Cerebro-costo-mandibulair syndroom</Name>
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-      <OrphaCode>139441</OrphaCode>
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-      <Name lang="nl">Leuko-encefalopathie met bilaterale anterieure temporaalkwabcysten</Name>
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-      <Name lang="nl">Progressieve caviterende leuko-encefalopathie</Name>
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-      <Name lang="nl">Stapes-ankylose met brede duimen en tenen</Name>
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-      <Name lang="nl">Cryptomicrotie - brachydactylie - excessieve vingertopboog-syndroom</Name>
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-      <OrphaCode>140922</OrphaCode>
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-      <Name lang="nl">Titine-gerelateerde limb-girdle-spierdystrofie R10</Name>
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-      <Name lang="nl">Syndroom van Crisponi</Name>
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-      <OrphaCode>140905</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=140905</ExpertLink>
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-          <Name lang="nl">No data available</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=140908</ExpertLink>
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-      <Name lang="nl">Syndroom van Gómez-López-Hernández</Name>
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-      <OrphaCode>1509</OrphaCode>
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-      <Name lang="nl">Coxopodopatellair syndroom</Name>
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-      <Name lang="nl">Syndroom van Crane-Heise</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <OrphaCode>140474</OrphaCode>
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-      <Name lang="nl">Autosomaal dominante erfelijke sensorische en autonome neuropathie</Name>
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-      <Name lang="nl">Autosomaal recessieve erfelijke sensorische en autonome neuropathie</Name>
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-        <Name lang="nl">Categorie</Name>
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-      <Name lang="nl">Dunne ribben - kokervormige botten - dysmorfie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>140456</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=140456</ExpertLink>
-      <Name lang="nl">Autosomaal dominante erfelijke axonale motorische en sensorische neuropathie</Name>
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-        <Name lang="nl">Categorie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=140459</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve erfelijke demyeliniserende motorische en sensorische neuropathie</Name>
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-        <Name lang="nl">Categorie</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <OrphaCode>1508</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1508</ExpertLink>
-      <Name lang="nl">Coxo-auriculair syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Autosomaal dominante distale erfelijke motorische neuropathie</Name>
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-        <Name lang="nl">Categorie</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <Name lang="nl">Autosomaal recessief syndroom van Robinow</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1517</ExpertLink>
-      <Name lang="nl">Syndroom van Cantú</Name>
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-      <Name lang="nl">Craniofrontonasale dysplasie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1513</ExpertLink>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1913">
-      <OrphaCode>1969</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1969</ExpertLink>
-      <Name lang="nl">Faciale dysmorfie - anorexie - cachexie - oog- en huidanomalieën-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1912">
-      <OrphaCode>1968</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1968</ExpertLink>
-      <Name lang="nl">Plat gelaat - microstomie - ooranomalie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1914">
-      <OrphaCode>1970</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1970</ExpertLink>
-      <Name lang="nl">Faciale dysmorfie - macrocefalie - myopie - Dandy-Walker malformatie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1917">
-      <OrphaCode>1973</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1973</ExpertLink>
-      <Name lang="nl">Faciocardiorenaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1916">
-      <OrphaCode>1972</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1972</ExpertLink>
-      <Name lang="nl">Letale facio-cardio-melische dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1918">
-      <OrphaCode>1974</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1974</ExpertLink>
-      <Name lang="nl">Autosomaal recessief faciodigitogenitaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1907">
-      <OrphaCode>1962</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1962</ExpertLink>
-      <Name lang="nl">Exostose - anetodermie - brachydactylie type E-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1908">
-      <OrphaCode>1964</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1964</ExpertLink>
-      <Name lang="nl">Extrasystolen - kleine gestalte - hyperpigmentatie - microcefalie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1896">
-      <OrphaCode>1822</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1822</ExpertLink>
-      <Name lang="nl">Dysplasia epiphysealis hemimelica</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1897">
-      <OrphaCode>1824</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1824</ExpertLink>
-      <Name lang="nl">Syndroom van Lowry-Wood</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1899">
-      <OrphaCode>1952</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1952</ExpertLink>
-      <Name lang="nl">Epifysaire stippeling - osteoclastische hyperplasie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1901">
-      <OrphaCode>1954</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1954</ExpertLink>
-      <Name lang="nl">Congenitale letale erytrodermie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1902">
-      <OrphaCode>1955</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1955</ExpertLink>
-      <Name lang="nl">Spinocerebellaire ataxie type 34</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1888">
-      <OrphaCode>1926</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1926</ExpertLink>
-      <Name lang="nl">Diabetische embryopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1889">
-      <OrphaCode>2209</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2209</ExpertLink>
-      <Name lang="nl">Maternale fenylketonurie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1890">
-      <OrphaCode>1927</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1927</ExpertLink>
-      <Name lang="nl">Syndroom van Emery-Nelson</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1891">
-      <OrphaCode>1937</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1937</ExpertLink>
-      <Name lang="nl">Syndroom van Eng-Strom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1882">
-      <OrphaCode>1920</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1920</ExpertLink>
-      <Name lang="nl">Tolueen-embryopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1881">
-      <OrphaCode>1919</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1919</ExpertLink>
-      <Name lang="nl">Fenobarbital-embryopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1880">
-      <OrphaCode>1917</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1917</ExpertLink>
-      <Name lang="nl">Foetaal methylkwiksyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1885">
-      <OrphaCode>1923</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1923</ExpertLink>
-      <Name lang="nl">Methimazol-embryofoetopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1875">
-      <OrphaCode>1912</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1912</ExpertLink>
-      <Name lang="nl">Foetaal hydantoïnesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1874">
-      <OrphaCode>1918</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1918</ExpertLink>
-      <Name lang="nl">Foetaal minoxidilsyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1873">
-      <OrphaCode>1911</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1911</ExpertLink>
-      <Name lang="nl">Cocaïne-embryofoetopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1872">
-      <OrphaCode>1910</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1910</ExpertLink>
-      <Name lang="nl">Foetaal jodiumsyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1879">
-      <OrphaCode>1916</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1916</ExpertLink>
-      <Name lang="nl">Diëthylstilbestrolsyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1878">
-      <OrphaCode>294</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=294</ExpertLink>
-      <Name lang="nl">Foetaal cytomegalovirussyndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1877">
-      <OrphaCode>1914</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1914</ExpertLink>
-      <Name lang="nl">Vitamine K-antagonisten-embryofoetopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1876">
-      <OrphaCode>1913</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1913</ExpertLink>
-      <Name lang="nl">Foetaal trimethadionsyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1864">
-      <OrphaCode>1896</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1896</ExpertLink>
-      <Name lang="nl">EEC-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1865">
-      <OrphaCode>1897</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1897</ExpertLink>
-      <Name lang="nl">EEM-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1870">
-      <OrphaCode>1908</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1908</ExpertLink>
-      <Name lang="nl">Aminopterine/methotrexaat-embryofoetopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1871">
-      <OrphaCode>1909</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1909</ExpertLink>
-      <Name lang="nl">Indometacine-embryofoetopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1868">
-      <OrphaCode>1906</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1906</ExpertLink>
-      <Name lang="nl">Foetaal valproaat-spectrumstoornis</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1863">
-      <OrphaCode>1895</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1895</ExpertLink>
-      <Name lang="nl">Edinburgh-malformatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1860">
-      <OrphaCode>1891</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1891</ExpertLink>
-      <Name lang="nl">Intellectuele achterstand - spasticiteit - ectrodactylie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1861">
-      <OrphaCode>1892</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1892</ExpertLink>
-      <Name lang="nl">Ectrodactylie - polydactylie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1853">
-      <OrphaCode>1816</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1816</ExpertLink>
-      <Name lang="nl">Leukomelanodermie - infantilisme - intellectuele achterstand - hypodontie - hypotrichose-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1855">
-      <OrphaCode>1807</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1807</ExpertLink>
-      <Name lang="nl">Focale faciale dermale dysplasie type III</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1854">
-      <OrphaCode>1818</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1818</ExpertLink>
-      <Name lang="nl">Ectodermale dysplasie, tricho-odonto-onychiaal type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1851">
-      <OrphaCode>1883</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1883</ExpertLink>
-      <Name lang="nl">Ectodermale dysplasie - sensorineurale doofheid-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1850">
-      <OrphaCode>1882</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1882</ExpertLink>
-      <Name lang="nl">Hypohidrotische ectodermale dysplasie - hypothyreoïdie - ciliaire dyskinesie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1845">
-      <OrphaCode>1875</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1875</ExpertLink>
-      <Name lang="nl">Congenitale spierdystrofie - infantiel cataract - hypogonadisme-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1844">
-      <OrphaCode>1873</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1873</ExpertLink>
-      <Name lang="nl">Syndroom van Jalili</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1847">
-      <OrphaCode>1879</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1879</ExpertLink>
-      <Name lang="nl">Melorheostose met osteopoikilose</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1840">
-      <OrphaCode>1867</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1867</ExpertLink>
-      <Name lang="nl">Erfelijke bulleuze dystrofie, maculair type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23431">
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-    <Disorder id="1843">
-      <OrphaCode>1872</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1872</ExpertLink>
-      <Name lang="nl">Kegel-staafdystrofie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1842">
-      <OrphaCode>1871</OrphaCode>
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-      <Name lang="nl">Progressieve kegeldystrofie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1837">
-      <OrphaCode>1860</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1860</ExpertLink>
-      <Name lang="nl">Thanatofore dysplasie type 1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-      <OrphaCode>1861</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1861</ExpertLink>
-      <Name lang="nl">Thoracale dysplasie - hydrocefalie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <OrphaCode>1865</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1865</ExpertLink>
-      <Name lang="nl">Dyssegmentale dysplasie, Silverman-Handmaker-type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1835">
-      <OrphaCode>1858</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1858</ExpertLink>
-      <Name lang="nl">Skeletdysplasie - epilepsie - kleine gestalte-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>254</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254</ExpertLink>
-      <Name lang="nl">Spondylometafysaire dysplasie</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1826">
-      <OrphaCode>1852</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1852</ExpertLink>
-      <Name lang="nl">X-gebonden retinale dysplasie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <OrphaCode>1842</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1842</ExpertLink>
-      <Name lang="nl">Botdysplasie, letaal Holmgren-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1818">
-      <OrphaCode>1839</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1839</ExpertLink>
-      <Name lang="nl">Erfelijke muco-epitheliale dysplasie</Name>
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-      <OrphaCode>1837</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1837</ExpertLink>
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-          <Name lang="nl">Neonataal</Name>
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-    </Disorder>
-    <Disorder id="2025">
-      <OrphaCode>2115</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2115</ExpertLink>
-      <Name lang="nl">Syndroom van Harrod</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2024">
-      <OrphaCode>2114</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2114</ExpertLink>
-      <Name lang="nl">Heupdysplasie, Beukes-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2027">
-      <OrphaCode>2994</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2994</ExpertLink>
-      <Name lang="nl">Kleine gestalte - craniofaciale anomalieën - genitale hypoplasie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2026">
-      <OrphaCode>2117</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2117</ExpertLink>
-      <Name lang="nl">Syndroom van Hartsfield</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2028">
-      <OrphaCode>2119</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2119</ExpertLink>
-      <Name lang="nl">HEC-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2030">
-      <OrphaCode>2123</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2123</ExpertLink>
-      <Name lang="nl">Diffuse neonatale hemangiomatose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17171">
-      <OrphaCode>157997</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157997</ExpertLink>
-      <Name lang="nl">Benigne cefale histiocytose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2002">
-      <OrphaCode>2090</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2090</ExpertLink>
-      <Name lang="nl">GMS-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17170">
-      <OrphaCode>157991</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157991</ExpertLink>
-      <Name lang="nl">Gegeneraliseerde eruptieve histiocytose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2003">
-      <OrphaCode>2091</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2091</ExpertLink>
-      <Name lang="nl">Multinodulair struma - cystische nier - polydactylie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17175">
-      <OrphaCode>158011</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158011</ExpertLink>
-      <Name lang="nl">Necrobiotisch xanthogranuloom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17174">
-      <OrphaCode>158008</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158008</ExpertLink>
-      <Name lang="nl">Papulair xanthoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="5">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2007">
-      <OrphaCode>376</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=376</ExpertLink>
-      <Name lang="nl">Syndroom van Gordon</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17173">
-      <OrphaCode>158003</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158003</ExpertLink>
-      <Name lang="nl">Xanthoma disseminatum</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2004">
-      <OrphaCode>2092</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2092</ExpertLink>
-      <Name lang="nl">Focale dermale hypoplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17172">
-      <OrphaCode>158000</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158000</ExpertLink>
-      <Name lang="nl">Juveniel xanthogranuloom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2010">
-      <OrphaCode>2098</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2098</ExpertLink>
-      <Name lang="nl">Acromesomele dysplasie, Grebe-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17179">
-      <OrphaCode>158025</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158025</ExpertLink>
-      <Name lang="nl">Hereditaire progressieve mucineuze histiocytose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17178">
-      <OrphaCode>158022</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158022</ExpertLink>
-      <Name lang="nl">Progressieve nodulaire histiocytose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2011">
-      <OrphaCode>380</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=380</ExpertLink>
-      <Name lang="nl">Greig-cefalopolysyndactyliesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2008">
-      <OrphaCode>2095</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2095</ExpertLink>
-      <Name lang="nl">Syndroom van Gorlin-Chaudhry-Moss</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17177">
-      <OrphaCode>158019</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158019</ExpertLink>
-      <Name lang="nl">Onbepaalde celhistiocytose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17176">
-      <OrphaCode>158014</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158014</ExpertLink>
-      <Name lang="nl">Ziekte van Rosaï-Dorfman</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="2009">
-      <OrphaCode>2097</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2097</ExpertLink>
-      <Name lang="nl">Syndroom van Grant</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="2014">
-      <OrphaCode>2101</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2101</ExpertLink>
-      <Name lang="nl">Syndroom van Grubben-de Cock-Borghgraef</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2015">
-      <OrphaCode>2104</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2104</ExpertLink>
-      <Name lang="nl">Dysmorfie - pectus carinatum - gewrichtslaxiteit-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="17181">
-      <OrphaCode>158032</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158032</ExpertLink>
-      <Name lang="nl">Hemofagocytair syndroom</Name>
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-        <Name lang="nl">Categorie</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="1987">
-      <OrphaCode>2069</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2069</ExpertLink>
-      <Name lang="nl">Gastrocutaan syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17155">
-      <OrphaCode>157846</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157846</ExpertLink>
-      <Name lang="nl">Neuroferritinopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17152">
-      <OrphaCode>157832</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157832</ExpertLink>
-      <Name lang="nl">Craniorhinie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1985">
-      <OrphaCode>2067</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2067</ExpertLink>
-      <Name lang="nl">GAPO-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="17153">
-      <OrphaCode>157835</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157835</ExpertLink>
-      <Name lang="nl">Paroxysmale hemicranie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="1984">
-      <OrphaCode>2065</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2065</ExpertLink>
-      <Name lang="nl">Syndroom van Galloway-Mowat</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1991">
-      <OrphaCode>2075</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2075</ExpertLink>
-      <Name lang="nl">Genitopalatocardiaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17159">
-      <OrphaCode>157941</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157941</ExpertLink>
-      <Name lang="nl">Ziekte van Huntington-achtig 1</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="1990">
-      <OrphaCode>2074</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2074</ExpertLink>
-      <Name lang="nl">Syndroom van Gemignani</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="17156">
-      <OrphaCode>157850</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157850</ExpertLink>
-      <Name lang="nl">Pantothenaatkinasegeassocieerde neurodegeneratie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="1989">
-      <OrphaCode>2072</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2072</ExpertLink>
-      <Name lang="nl">Ziekte van Gaucher - oftalmoplegie - cardiovasculaire calcificatie-syndroom</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="17162">
-      <OrphaCode>157954</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157954</ExpertLink>
-      <Name lang="nl">ANE-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="17163">
-      <OrphaCode>157962</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157962</ExpertLink>
-      <Name lang="nl">Oculo-auriculair syndroom, Schorderet-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="17160">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157946</ExpertLink>
-      <Name lang="nl">Ziekte van Huntington-achtig 3</Name>
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-        <Name lang="nl">Ziekte</Name>
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-    <Disorder id="1993">
-      <OrphaCode>2078</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2078</ExpertLink>
-      <Name lang="nl">Geroderma osteodysplastica</Name>
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-      <OrphaCode>157949</OrphaCode>
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-      <Name lang="nl">Gecombineerde immuundeficiëntie met granulomatose</Name>
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-    <Disorder id="1992">
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-      <Name lang="nl">Syndroom van German</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Congenitale spierdystrofie door LMNA-mutatie</Name>
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-        <AverageAgeOfOnset id="23515">
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-      <OrphaCode>2084</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2084</ExpertLink>
-      <Name lang="nl">Glaucoom - ectopia lentis - microsferofakie - stijve gewrichten - kleine gestalte-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="17164">
-      <OrphaCode>157965</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=157965</ExpertLink>
-      <Name lang="nl">SLC39A13-gerelateerd spondylodysplastisch syndroom van Ehlers-Danlos</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1997">
-      <OrphaCode>2083</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2083</ExpertLink>
-      <Name lang="nl">Prominente glabella - microcefalie - hypogenitalisme-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1974">
-      <OrphaCode>1791</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1791</ExpertLink>
-      <Name lang="nl">Fronto-facio-nasale dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1975">
-      <OrphaCode>1826</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1826</ExpertLink>
-      <Name lang="nl">Frontometafysaire dysplasie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1968">
-      <OrphaCode>2047</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2047</ExpertLink>
-      <Name lang="nl">Syndroom van Flynn-Aird</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1969">
-      <OrphaCode>2048</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2048</ExpertLink>
-      <Name lang="nl">Syndroom van Foix-Chavany-Marie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1971">
-      <OrphaCode>2050</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2050</ExpertLink>
-      <Name lang="nl">Syndroom van Cole-Carpenter</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="3">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1982">
-      <OrphaCode>2063</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2063</ExpertLink>
-      <Name lang="nl">Splenogonadale fusie - ledemaatdefecten - micrognatie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1983">
-      <OrphaCode>2064</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2064</ExpertLink>
-      <Name lang="nl">Posterieure fusie van lumbosacrale wervels - blefaroptose-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1976">
-      <OrphaCode>250</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=250</ExpertLink>
-      <Name lang="nl">Frontonasale dysplasie</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1978">
-      <OrphaCode>2057</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2057</ExpertLink>
-      <Name lang="nl">Blefarofimose - ptose - esotropie - syndactylie - kleine gestalte-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1979">
-      <OrphaCode>2059</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2059</ExpertLink>
-      <Name lang="nl">Syndroom van Fryns</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1957">
-      <OrphaCode>2026</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2026</ExpertLink>
-      <Name lang="nl">Gingivale fibromatose - hypertrichose-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1956">
-      <OrphaCode>2025</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2025</ExpertLink>
-      <Name lang="nl">Gingivale fibromatose - faciale dysmorfie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1959">
-      <OrphaCode>2028</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2028</ExpertLink>
-      <Name lang="nl">Juveniele hyaliene fibromatose</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1958">
-      <OrphaCode>2027</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2027</ExpertLink>
-      <Name lang="nl">Gingivale fibromatose - progressieve doofheid-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1953">
-      <OrphaCode>2021</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2021</ExpertLink>
-      <Name lang="nl">Fibrochondrogenese</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1952">
-      <OrphaCode>2019</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2019</ExpertLink>
-      <Name lang="nl">Femur-fibula-ulna-complex</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1955">
-      <OrphaCode>2024</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2024</ExpertLink>
-      <Name lang="nl">Erfelijke gingivale fibromatose</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1954">
-      <OrphaCode>2022</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2022</ExpertLink>
-      <Name lang="nl">Endocardiale fibro-elastose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1965">
-      <OrphaCode>2824</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2824</ExpertLink>
-      <Name lang="nl">Paraplegie - intellectuele achterstand - hyperkeratose-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="1967">
-      <OrphaCode>2045</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2045</ExpertLink>
-      <Name lang="nl">FLOTCH-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="1966">
-      <OrphaCode>2044</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2044</ExpertLink>
-      <Name lang="nl">Floating-Harbor-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <Name lang="nl">Typische urticaria pigmentosa</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <OrphaCode>2007</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2007</ExpertLink>
-      <Name lang="nl">Hypoplasie van kraakbeen van neusvleugel - coloboom - telecanthus-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2003</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2003</ExpertLink>
-      <Name lang="nl">Gespleten lip/gehemelte - doofheid - sacraal lipoom-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Unknown</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="17237">
-      <OrphaCode>158687</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158687</ExpertLink>
-      <Name lang="nl">Letale acantholytische erosieve aandoening</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="17236">
-      <OrphaCode>158684</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158684</ExpertLink>
-      <Name lang="nl">Epidermolysis bullosa simplex met pylorusatresie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="1941">
-      <OrphaCode>2004</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2004</ExpertLink>
-      <Name lang="nl">Laryngo-tracheo-oesofageale fissuur</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2001</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2001</ExpertLink>
-      <Name lang="nl">Gespleten lip/verhemelte - intestinale malrotatie - cardiopathie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="17235">
-      <OrphaCode>158681</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=158681</ExpertLink>
-      <Name lang="nl">Epidermolysis bullosa simplex met circinair migrerend erytheem</Name>
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-      <Name lang="nl">Nodulaire urticaria pigmentosa</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2008</ExpertLink>
-      <Name lang="nl">Acrocardiofaciaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="1927">
-      <OrphaCode>1987</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1987</ExpertLink>
-      <Name lang="nl">Geïsoleerde agenesie/hypoplasie van femur</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1926">
-      <OrphaCode>1986</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1986</ExpertLink>
-      <Name lang="nl">Gollop-Wolfgangcomplex</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="1923">
-      <OrphaCode>1980</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1980</ExpertLink>
-      <Name lang="nl">Bilaterale striatopallidodentate calcinose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="3">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1934">
-      <OrphaCode>1997</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1997</ExpertLink>
-      <Name lang="nl">Blefaro-cheilo-odontisch syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1932">
-      <OrphaCode>1995</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1995</ExpertLink>
-      <Name lang="nl">Gespleten lip - retinopathie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="1931">
-      <OrphaCode>1993</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1993</ExpertLink>
-      <Name lang="nl">Syndroom van Pai</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="1928">
-      <OrphaCode>1988</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1988</ExpertLink>
-      <Name lang="nl">Femoraal-faciaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="2200">
-      <OrphaCode>2348</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2348</ExpertLink>
-      <Name lang="nl">Familiale partiële lipodystrofie, Dunnigan-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="19545">
-      <OrphaCode>247775</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247775</ExpertLink>
-      <Name lang="nl">Syndroom van Mayer-Rokitansky-Küster-Hauser type 1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="19544">
-      <OrphaCode>247768</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247768</ExpertLink>
-      <Name lang="nl">Mülleriaanse aplasie en hyperandrogenisme</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2201">
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-      <Name lang="nl">Syndroom van Kousseff</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2353</OrphaCode>
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-      <Name lang="nl">Syndroom van Schilbach-Rott</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">No data available</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247798</ExpertLink>
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-        <AverageAgeOfOnset id="23543">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247794</ExpertLink>
-      <Name lang="nl">Juveniel cataract - microcornea - renale glucosurie-syndroom</Name>
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-    <Disorder id="19551">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247815</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve ataxie door PEX10-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <AverageAgeOfOnset id="23536">
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <Name lang="nl">Lacrimo-auriculo-dento-digitaal syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <OrphaCode>247691</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247691</ExpertLink>
-      <Name lang="nl">Retinale vasculopathie met cerebrale leuko-encefalopathie en systemische manifestaties</Name>
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-      <Name lang="nl">Syndroom van Haim-Munk</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <OrphaCode>247709</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247709</ExpertLink>
-      <Name lang="nl">Multipele endocriene neoplasie type 2B</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="19538">
-      <OrphaCode>247698</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247698</ExpertLink>
-      <Name lang="nl">Multipele endocriene neoplasie type 2A</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      <OrphaCode>247724</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247724</ExpertLink>
-      <Name lang="nl">Idiopathische eosinofiele myositis</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <TypeOfInheritance id="23494">
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-      <OrphaCode>247718</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247718</ExpertLink>
-      <Name lang="nl">Inflammatoire myopathie met abundante macrofagen</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="19543">
-      <OrphaCode>247765</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247765</ExpertLink>
-      <Name lang="nl">X-gebonden cerebellaire ataxie</Name>
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-        <Name lang="nl">Categorie</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <TypeOfInheritanceList count="2">
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-          <Name lang="nl">X-gebonden dominant</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="2198">
-      <OrphaCode>485</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=485</ExpertLink>
-      <Name lang="nl">Kniestdysplasie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="19542">
-      <OrphaCode>247762</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247762</ExpertLink>
-      <Name lang="nl">Lipoblastoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      <OrphaCode>2347</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2347</ExpertLink>
-      <Name lang="nl">Letale Kniest-achtige dysplasie</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19528">
-      <OrphaCode>247585</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247585</ExpertLink>
-      <Name lang="nl">Citrullinemie type II</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2185">
-      <OrphaCode>2333</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2333</ExpertLink>
-      <Name lang="nl">Syndroom van Kenny-Caffey</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19529">
-      <OrphaCode>247598</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247598</ExpertLink>
-      <Name lang="nl">Neonatale intrahepatische cholestase door deficiëntie van citrine</Name>
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-      <OrphaCode>2332</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2332</ExpertLink>
-      <Name lang="nl">KBG-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <OrphaCode>247604</OrphaCode>
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-      <Name lang="nl">Sporadische ataxie met aanvang op volwassen leeftijd met onbekende etiologie</Name>
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-      <Name lang="nl">Syndroom van Melkersson-Rosenthal</Name>
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-      <Name lang="nl">Verzamelkanaalcarcinoom</Name>
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-      <Name lang="nl">Syndroom van Melnick-Needles</Name>
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-      <OrphaCode>247198</OrphaCode>
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-      <Name lang="nl">Progressieve cerebello-cerebrale atrofie</Name>
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-      <Name lang="nl">Neurocutane melanocytose</Name>
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-      <Name lang="nl">Syndroom van Melhem-Fahl</Name>
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-      <Name lang="nl">Infantiele kwikvergiftiging</Name>
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-      <Name lang="nl">Witte voorhoofdslok met misvormingen</Name>
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-      <Name lang="nl">Dysrafie - gespleten lip/verhemelte - reductiedefect van ledemaat-syndroom</Name>
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-      <Name lang="nl">Syndroom van McKusick-Kaufman</Name>
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-    <Disorder id="19666">
-      <OrphaCode>251636</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251636</ExpertLink>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="19667">
-      <OrphaCode>251639</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251639</ExpertLink>
-      <Name lang="nl">Subependymoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="19668">
-      <OrphaCode>251643</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251643</ExpertLink>
-      <Name lang="nl">Myxopapillair ependymoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23557">
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2069">
-      <OrphaCode>2176</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2176</ExpertLink>
-      <Name lang="nl">Infantiele systemische hyalinose</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19669">
-      <OrphaCode>251646</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251646</ExpertLink>
-      <Name lang="nl">Anaplastisch ependymoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2071">
-      <OrphaCode>2181</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2181</ExpertLink>
-      <Name lang="nl">Hydrocefalie - grote gestalte - gewrichtslaxiteit-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2070">
-      <OrphaCode>2180</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2180</ExpertLink>
-      <Name lang="nl">Hydrocefalus - costovertebrale dysplasie - anomalie van Sprengel-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
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-    <Disorder id="19672">
-      <OrphaCode>251663</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251663</ExpertLink>
-      <Name lang="nl">Anaplastisch oligoastrocytoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2072">
-      <OrphaCode>2186</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2186</ExpertLink>
-      <Name lang="nl">Hydrocefalus - blauwe sclerae - nefropathie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="19674">
-      <OrphaCode>251671</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251671</ExpertLink>
-      <Name lang="nl">Angiocentrisch glioom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="2075">
-      <OrphaCode>2189</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2189</ExpertLink>
-      <Name lang="nl">Hydrolethalus</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19675">
-      <OrphaCode>251674</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251674</ExpertLink>
-      <Name lang="nl">Chordoïd glioom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="19676">
-      <OrphaCode>251679</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251679</ExpertLink>
-      <Name lang="nl">Astroblastoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="2079">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=312</ExpertLink>
-      <Name lang="nl">Autosomaal dominante epidermolytische ichthyosis</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2196</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2196</ExpertLink>
-      <Name lang="nl">Primaire hypomagnesiëmie met hypercalciurie en nefrocalcinose met ernstige oculaire betrokkenheid</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <AverageAgeOfOnset id="23529">
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-    <Disorder id="19649">
-      <OrphaCode>251576</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251576</ExpertLink>
-      <Name lang="nl">Gliosarcoom</Name>
-      <DisorderType id="21457">
-        <Name lang="nl">Histopathologisch subtype</Name>
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-      <AverageAgeOfOnsetList count="1">
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-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="2050">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2150</ExpertLink>
-      <Name lang="nl">Ziekte van Hirschsprung - brachydactylie type D-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23515">
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-    <Disorder id="19651">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251582</ExpertLink>
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-          <Name lang="nl">Volwassenheid</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251579</ExpertLink>
-      <Name lang="nl">Reuscelglioblastoom</Name>
-      <DisorderType id="21457">
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-          <Name lang="nl">Volwassenheid</Name>
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-      <Name lang="nl">Syndroom van Mowat-Wilson</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2153</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2153</ExpertLink>
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-        <AverageAgeOfOnset id="23515">
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
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-    <Disorder id="19652">
-      <OrphaCode>251589</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251589</ExpertLink>
-      <Name lang="nl">Anaplastisch astrocytoom</Name>
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-        <AverageAgeOfOnset id="23543">
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-      <Name lang="nl">Protoplasmisch astrocytoom</Name>
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-        <Name lang="nl">Histopathologisch subtype</Name>
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-        <AverageAgeOfOnset id="23529">
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-        <TypeOfInheritance id="23494">
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-      <Name lang="nl">Ziekte van Hirschsprung - doofheid - polydactylie-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2158</ExpertLink>
-      <Name lang="nl">Histidinurie - defect van niertubulus-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251612</ExpertLink>
-      <Name lang="nl">Pilocytair astrocytoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251607</ExpertLink>
-      <Name lang="nl">Pleomorf xanthoastrocytoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2165</ExpertLink>
-      <Name lang="nl">Holoprosencefalie - caudale dysgenesie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251615</ExpertLink>
-      <Name lang="nl">Pilomyxoid astrocytoom</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>2166</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2166</ExpertLink>
-      <Name lang="nl">Holoprosencefalie - postaxiale polydactylie-syndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="19663">
-      <OrphaCode>251627</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251627</ExpertLink>
-      <Name lang="nl">Oligodendroglioom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2167</ExpertLink>
-      <Name lang="nl">Syndroom van Holzgreve</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251623</ExpertLink>
-      <Name lang="nl">Pituïcytoom</Name>
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-      <Name lang="nl">Methylcobalaminedeficiëntie type cblE</Name>
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-      <Name lang="nl">Cerebellair liponeurocytoom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <OrphaCode>2222</OrphaCode>
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-      <Name lang="nl">Hypertrichosis lanuginosa congenita</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251940</ExpertLink>
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-      <Name lang="nl">Familiale geïsoleerde hypoparathyreoïdie</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-      <OrphaCode>2237</OrphaCode>
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-      <Name lang="nl">Hypoparathyreoïdie - sensorineurale doofheid - nierziekte-syndroom</Name>
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-      <Name lang="nl">Hypogonadotroop hypogonadisme - retinitis pigmentosa-syndroom</Name>
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-          <Name lang="nl">No data available</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251992</ExpertLink>
-      <Name lang="nl">Ganglioneuroom</Name>
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-      <Name lang="nl">Mannelijk hypergonadotroop hypogonadisme - intellectuele achterstand - skeletanomalieën-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="2095">
-      <OrphaCode>2218</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2218</ExpertLink>
-      <Name lang="nl">Cervicale hypertrichose - perifere neuropathie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="19693">
-      <OrphaCode>251909</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251909</ExpertLink>
-      <Name lang="nl">Pineoblastoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2092">
-      <OrphaCode>2215</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2215</ExpertLink>
-      <Name lang="nl">Meervoudig pterygium - maligne hyperthermie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="2093">
-      <OrphaCode>2216</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2216</ExpertLink>
-      <Name lang="nl">Geboortedefecten geïnduceerd door maternale hyperthermie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19604">
-      <OrphaCode>251019</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251019</ExpertLink>
-      <Name lang="nl">2q32q33-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2133">
-      <OrphaCode>2266</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2266</ExpertLink>
-      <Name lang="nl">Hypotrichose-intellectuele achterstand, Lopes-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19605">
-      <OrphaCode>251028</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251028</ExpertLink>
-      <Name lang="nl">SATB2-geassocieerd syndroom door een chromosomale herschikking</Name>
-      <DisorderType id="21443">
-        <Name lang="nl">Etiologisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2135">
-      <OrphaCode>2269</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2269</ExpertLink>
-      <Name lang="nl">Ichthyosis - alopecie - eclabium - ectropion - intellectuele achterstand-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="19607">
-      <OrphaCode>251038</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251038</ExpertLink>
-      <Name lang="nl">3q29-microduplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="19600">
-      <OrphaCode>250999</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=250999</ExpertLink>
-      <Name lang="nl">1q41q42-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
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-    </Disorder>
-    <Disorder id="2129">
-      <OrphaCode>2261</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2261</ExpertLink>
-      <Name lang="nl">Hypospadie - intellectuele achterstand-syndroom, Goldblatt-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="19601">
-      <OrphaCode>251004</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251004</ExpertLink>
-      <Name lang="nl">Paternale uniparentale disomie van chromosoom 1-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="19602">
-      <OrphaCode>251009</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251009</ExpertLink>
-      <Name lang="nl">Maternale uniparentale disomie van chromosoom 1-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="2130">
-      <OrphaCode>672</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=672</ExpertLink>
-      <Name lang="nl">Syndroom van Pallister-Hall</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      </DisorderGroup>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="19603">
-      <OrphaCode>251014</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251014</ExpertLink>
-      <Name lang="nl">2q31.1-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
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-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="2141">
-      <OrphaCode>455</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=455</ExpertLink>
-      <Name lang="nl">Oppervlakkige epidermolytische ichthyosis</Name>
-      <DisorderType id="21394">
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-        <AverageAgeOfOnset id="23522">
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="19612">
-      <OrphaCode>251061</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251061</ExpertLink>
-      <Name lang="nl">7q31-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
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-    <Disorder id="19613">
-      <OrphaCode>251066</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251066</ExpertLink>
-      <Name lang="nl">8p11.2-deletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
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-    <Disorder id="2140">
-      <OrphaCode>2272</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2272</ExpertLink>
-      <Name lang="nl">Ichthyosis - orale en digitale anomalieën-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19614">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251071</ExpertLink>
-      <Name lang="nl">8p23.1-microdeletiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
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-    <Disorder id="2143">
-      <OrphaCode>2274</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2274</ExpertLink>
-      <Name lang="nl">Ichthyosis - hepatosplenomegalie - cerebellaire degeneratie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    </Disorder>
-    <Disorder id="19615">
-      <OrphaCode>251076</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251076</ExpertLink>
-      <Name lang="nl">8p23.1-duplicatiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    </Disorder>
-    <Disorder id="2142">
-      <OrphaCode>2273</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2273</ExpertLink>
-      <Name lang="nl">Folliculaire ichthyosis - alopecie - fotofobie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="19608">
-      <OrphaCode>251043</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251043</ExpertLink>
-      <Name lang="nl">Ringchromosoom 5-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2137">
-      <OrphaCode>165</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=165</ExpertLink>
-      <Name lang="nl">Neutrale vetstapelingsziekte</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2136">
-      <OrphaCode>139</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=139</ExpertLink>
-      <Name lang="nl">CHILD-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19609">
-      <OrphaCode>251046</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251046</ExpertLink>
-      <Name lang="nl">6p22-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    </Disorder>
-    <Disorder id="2139">
-      <OrphaCode>457</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457</ExpertLink>
-      <Name lang="nl">Harlekijnichthyosis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2138">
-      <OrphaCode>2271</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2271</ExpertLink>
-      <Name lang="nl">Congenitale ichthyosis - microcefalus - tetraplegie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19611">
-      <OrphaCode>251056</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251056</ExpertLink>
-      <Name lang="nl">6q25.2q25.3-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
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-    </Disorder>
-    <Disorder id="2117">
-      <OrphaCode>2246</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2246</ExpertLink>
-      <Name lang="nl">Cerebellaire hypoplasie - tapetoretinale degeneratie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="19591">
-      <OrphaCode>250831</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=250831</ExpertLink>
-      <Name lang="nl">Logopenische progressieve afasie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2119">
-      <OrphaCode>2249</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2249</ExpertLink>
-      <Name lang="nl">Hypoplasie van ulna - intellectuele achterstand-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2112">
-      <OrphaCode>2239</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2239</ExpertLink>
-      <Name lang="nl">Familiale geïsoleerde hypoparathyreoïdie door agenesie van bijschildklier</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="2113">
-      <OrphaCode>2241</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2241</ExpertLink>
-      <Name lang="nl">Megacystis - microcolon - intestinale hypoperistaltiek-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19597">
-      <OrphaCode>250984</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=250984</ExpertLink>
-      <Name lang="nl">Autosomaal recessief syndroom van Stickler</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2124">
-      <OrphaCode>2256</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2256</ExpertLink>
-      <Name lang="nl">Fibulo-ulnaire hypoplasie - nieranomalieën-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="2125">
-      <OrphaCode>2257</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2257</ExpertLink>
-      <Name lang="nl">Primaire pulmonale hypoplasie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="19596">
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-      <Name lang="nl">AICA-ribosidurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19599">
-      <OrphaCode>250994</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=250994</ExpertLink>
-      <Name lang="nl">1q21.1-microduplicatiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="19598">
-      <OrphaCode>250989</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=250989</ExpertLink>
-      <Name lang="nl">1q21.1-microdeletiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-      <Name lang="nl">Pachyonychia congenita</Name>
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-      <Name lang="nl">Gelokaliseerde junctionele epidermolysis bullosa</Name>
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-      <Name lang="nl">Gepigmenteerde paraveneuze retinochoroïdale atrofie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=251290</ExpertLink>
-      <Name lang="nl">Foramina parietalia met hypoplasie van clavicula</Name>
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-      <Name lang="nl">Goedaardige concentrische annulaire maculadystrofie</Name>
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-      <Name lang="nl">Syndroom van Neuhauser-Eichner-Opitz</Name>
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-    <Disorder id="19790">
-      <OrphaCode>254857</OrphaCode>
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-      <Name lang="nl">Letale infantiele mitochondriale myopathie</Name>
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-      <Name lang="nl">Familiale geïsoleerde café-au-lait maculae</Name>
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-      <OrphaCode>254913</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254913</ExpertLink>
-      <Name lang="nl">Geïsoleerde ATP-synthasedeficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19807">
-      <OrphaCode>255182</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=255182</ExpertLink>
-      <Name lang="nl">Pyruvaatdehydrogenase E3-bindend proteïnedeficiëntie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2462">
-      <OrphaCode>2701</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2701</ExpertLink>
-      <Name lang="nl">Syndroom van Noonan-achtige aandoening met loszittend anageen haar</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19806">
-      <OrphaCode>255138</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=255138</ExpertLink>
-      <Name lang="nl">Pyruvaatdehydrogenase E1-bèta-deficiëntie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19805">
-      <OrphaCode>255132</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=255132</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve sideroblastische anemie met aanvang op volwassen leeftijd</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2460">
-      <OrphaCode>2698</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2698</ExpertLink>
-      <Name lang="nl">Knokkelkussens - leukonychie - sensorineurale doofheid - palmoplantaire hyperkeratose-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2461">
-      <OrphaCode>2699</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2699</ExpertLink>
-      <Name lang="nl">Mediane nodulus van bovenlip</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19795">
-      <OrphaCode>254886</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254886</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve progressieve externe oftalmoplegie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19794">
-      <OrphaCode>254881</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254881</ExpertLink>
-      <Name lang="nl">Spinocerebellaire ataxie met epilepsie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19793">
-      <OrphaCode>254875</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254875</ExpertLink>
-      <Name lang="nl">Mitochondriaal DNA-depletiesyndroom, myopathische vorm</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19792">
-      <OrphaCode>254871</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254871</ExpertLink>
-      <Name lang="nl">Mitochondriaal DNA-depletiesyndroom, hepatocerebrale vorm</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19799">
-      <OrphaCode>254905</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254905</ExpertLink>
-      <Name lang="nl">Geïsoleerde cytochroom C-oxidasedeficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23438">
-          <Name lang="nl">Mitochondriale overerving</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19798">
-      <OrphaCode>254902</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254902</ExpertLink>
-      <Name lang="nl">Renale tubulopathie - encefalopathie - leverfalen-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2452">
-      <OrphaCode>2690</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2690</ExpertLink>
-      <Name lang="nl">Neutropenie - monocytopenie - doofheid-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19797">
-      <OrphaCode>254898</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254898</ExpertLink>
-      <Name lang="nl">Doofheid - encefaloneuropathie - obesitas - valvulopathie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19796">
-      <OrphaCode>254892</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254892</ExpertLink>
-      <Name lang="nl">Autosomaal dominante progressieve externe oftalmoplegie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2473">
-      <OrphaCode>2712</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2712</ExpertLink>
-      <Name lang="nl">Oculofaciocardiodentaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2475">
-      <OrphaCode>2714</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2714</ExpertLink>
-      <Name lang="nl">Oculopalatocerebraal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2474">
-      <OrphaCode>2713</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2713</ExpertLink>
-      <Name lang="nl">Oculo-osteocutaan syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2476">
-      <OrphaCode>2715</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2715</ExpertLink>
-      <Name lang="nl">Ernstig oculo-reno-cerebellair syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2479">
-      <OrphaCode>2718</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2718</ExpertLink>
-      <Name lang="nl">Oculotrichodysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2478">
-      <OrphaCode>2717</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2717</ExpertLink>
-      <Name lang="nl">Oculo-tricho-anaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2465">
-      <OrphaCode>2704</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2704</ExpertLink>
-      <Name lang="nl">Urofaciaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2464">
-      <OrphaCode>2703</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2703</ExpertLink>
-      <Name lang="nl">Wijnvlekken - mega cisterna magna - hydrocefalus</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19809">
-      <OrphaCode>255210</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=255210</ExpertLink>
-      <Name lang="nl">Mitochondriaal DNA-geassocieerd syndroom van Leigh</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23438">
-          <Name lang="nl">Mitochondriale overerving</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="19812">
-      <OrphaCode>255229</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=255229</ExpertLink>
-      <Name lang="nl">Navajo neurohepatopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2468">
-      <OrphaCode>2707</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2707</ExpertLink>
-      <Name lang="nl">Oculo-cerebro-faciaal syndroom, Kaufman-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19813">
-      <OrphaCode>255235</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=255235</ExpertLink>
-      <Name lang="nl">Mitochondriaal DNA-depletiesyndroom, encefalomyopathische vorm met renale tubulopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2471">
-      <OrphaCode>2710</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2710</ExpertLink>
-      <Name lang="nl">Oculodentodigitale dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2470">
-      <OrphaCode>2709</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2709</ExpertLink>
-      <Name lang="nl">Oculodentaal syndroom, Rutherfurd-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2489">
-      <OrphaCode>2728</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2728</ExpertLink>
-      <Name lang="nl">Blefarofimose - intellectuele achterstand-syndroom, Ohdo-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2490">
-      <OrphaCode>2730</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2730</ExpertLink>
-      <Name lang="nl">Postaxiale tetramelische oligodactylie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2492">
-      <OrphaCode>2732</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2732</ExpertLink>
-      <Name lang="nl">Olivopontocerebellaire atrofie - doofheid-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="2493">
-      <OrphaCode>2733</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2733</ExpertLink>
-      <Name lang="nl">Omodysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="2480">
-      <OrphaCode>2719</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2719</ExpertLink>
-      <Name lang="nl">Oculocerebrale hypopigmentatie-syndroom, Cross-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2481">
-      <OrphaCode>2720</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2720</ExpertLink>
-      <Name lang="nl">Oculocerebrale hypopigmentatie-syndroom, Preus-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="2482">
-      <OrphaCode>2721</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2721</ExpertLink>
-      <Name lang="nl">Odonto-onycho-dermale dysplasie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2483">
-      <OrphaCode>2722</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2722</ExpertLink>
-      <Name lang="nl">Odonto-onycho dysplasie - alopecie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="2484">
-      <OrphaCode>2723</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2723</ExpertLink>
-      <Name lang="nl">Odontotrichomelisch syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2485">
-      <OrphaCode>2724</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2724</ExpertLink>
-      <Name lang="nl">Odontomatose - aortae esophagus stenosis-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="19831">
-      <OrphaCode>260305</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=260305</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve sideroblastische anemie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2511">
-      <OrphaCode>2755</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2755</ExpertLink>
-      <Name lang="nl">Orofaciodigitaal syndroom type 8</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="2510">
-      <OrphaCode>2754</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2754</ExpertLink>
-      <Name lang="nl">Orofaciodigitaal syndroom type 6</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-      <OrphaCode>252164</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=252164</ExpertLink>
-      <Name lang="nl">Goedaardig schwannoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2509">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2753</ExpertLink>
-      <Name lang="nl">Orofaciodigitaal syndroom type 4</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
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-        <AverageAgeOfOnset id="23508">
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-        <AverageAgeOfOnset id="23522">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-      <OrphaCode>2751</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2751</ExpertLink>
-      <Name lang="nl">Orofaciodigitaal syndroom type 2</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2506">
-      <OrphaCode>2750</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2750</ExpertLink>
-      <Name lang="nl">Orofaciodigitaal syndroom type 1</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19718">
-      <OrphaCode>252050</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=252050</ExpertLink>
-      <Name lang="nl">Primair melanoom van centraal zenuwstelsel</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2503">
-      <OrphaCode>2743</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2743</ExpertLink>
-      <Name lang="nl">Oftalmoplegie - intellectuele achterstand - lingua scrotalis-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19719">
-      <OrphaCode>252054</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=252054</ExpertLink>
-      <Name lang="nl">Hemangioblastoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2501">
-      <OrphaCode>2741</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2741</ExpertLink>
-      <Name lang="nl">Oftalmomandibulomele dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2497">
-      <OrphaCode>661</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=661</ExpertLink>
-      <Name lang="nl">Congenitale centrale hypoventilatie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2496">
-      <OrphaCode>2736</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2736</ExpertLink>
-      <Name lang="nl">Letale omfalocele - gespleten verhemelte-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19743">
-      <OrphaCode>254367</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254367</ExpertLink>
-      <Name lang="nl">Zeldzame lichen planus</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="2526">
-      <OrphaCode>2776</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2776</ExpertLink>
-      <Name lang="nl">Autosomaal recessief distale osteolyse-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2527">
-      <OrphaCode>2777</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2777</ExpertLink>
-      <Name lang="nl">Osteomesopycnose</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="19742">
-      <OrphaCode>254361</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254361</ExpertLink>
-      <Name lang="nl">Plectine-gerelateerde limb-girdle-spierdystrofie R17</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2524">
-      <OrphaCode>2774</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2774</ExpertLink>
-      <Name lang="nl">Multicentrische carpotarsale osteolyse met of zonder nefropathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="19740">
-      <OrphaCode>254351</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254351</ExpertLink>
-      <Name lang="nl">Distale 7q11.23-microdeletiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2522">
-      <OrphaCode>2769</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2769</ExpertLink>
-      <Name lang="nl">Familiale osteodysplasie, Anderson-type</Name>
-      <DisorderType id="21401">
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">19q13.12-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2523">
-      <OrphaCode>2770</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2770</ExpertLink>
-      <Name lang="nl">Ziekte van Nasu-Hakola</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254343</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve spastische ataxie - opticusatrofie - dysartrie-syndroom</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <OrphaCode>2767</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2767</ExpertLink>
-      <Name lang="nl">Carpotarsale osteochondromatose</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <OrphaCode>254334</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254334</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve intermediaire ziekte van Charcot-Marie-Tooth type B</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2521">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2768</ExpertLink>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2762</ExpertLink>
-      <Name lang="nl">Progressieve ossale heteroplasie</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-      <Name lang="nl">Osteocraniostenose</Name>
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-      <Name lang="nl">Constitutionele 'mismatch repair'-deficiëntie-syndroom</Name>
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-    <Disorder id="2514">
-      <OrphaCode>2759</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2759</ExpertLink>
-      <Name lang="nl">Ongeperforeerde orofarynx - costovertebrale anomalieën-syndroom</Name>
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-      <OrphaCode>2760</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2760</ExpertLink>
-      <Name lang="nl">OSLAM-syndroom</Name>
-      <DisorderType id="21401">
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=252183</ExpertLink>
-      <Name lang="nl">Neurofibroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254516</ExpertLink>
-      <Name lang="nl">Syndroom van Temple</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2793</ExpertLink>
-      <Name lang="nl">Oto-onycho-peroneaal syndroom</Name>
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-    <Disorder id="2540">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2792</ExpertLink>
-      <Name lang="nl">Otofaciocervicaal syndroom</Name>
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-      <Name lang="nl">Syndroom van Kagami-Ogata</Name>
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-      <Name lang="nl">Syndroom van Temple door paternale 14q32.2-microdeletie</Name>
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-      <Name lang="nl">Lichen planus pigmentosus</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <Name lang="nl">Osteopathia striata - craniale sclerose-syndroom</Name>
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-      <OrphaCode>667</OrphaCode>
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-      <Name lang="nl">X-gebonden sideroblastische anemie en spinocerebellaire ataxie</Name>
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-      <Name lang="nl">Syndroom van Temple door paternale 14q32.2-hypomethylatie</Name>
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-    <Disorder id="19763">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=254688</ExpertLink>
-      <Name lang="nl">Complete mola hydatidosa</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <Name lang="nl">W-syndroom</Name>
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-      <OrphaCode>2491</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2491</ExpertLink>
-      <Name lang="nl">Anomalieën van gang van Müller - ledemaatanomalieën-syndroom</Name>
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-      <Name lang="nl">FATCO-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <OrphaCode>2498</OrphaCode>
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-      <Name lang="nl">Syndactylie type 8</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2499</ExpertLink>
-      <Name lang="nl">Metachondromatose</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2497</OrphaCode>
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-      <Name lang="nl">Mesomele dysplasie van bovenste ledematen, Fryns-type</Name>
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-      <Name lang="nl">Metafysaire dysostose - intellectuele achterstand - conductieve doofheid-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2500</ExpertLink>
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-      <Name lang="nl">Microcefalie - gespleten verhemelte - abnormale retinale pigmentatie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="2329">
-      <OrphaCode>2518</OrphaCode>
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-      <Name lang="nl">Autosomaal recessief chorioretinopathie - microcefalie-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2524</OrphaCode>
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-      <Name lang="nl">Pontocerebellaire hypoplasie type 2</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2333">
-      <OrphaCode>2523</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2523</ExpertLink>
-      <Name lang="nl">Microcefalie - hersendefect - spasticiteit - hypernatriëmie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2522</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2522</ExpertLink>
-      <Name lang="nl">Microcefalie - fusie van cervicale wervelkolom-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2336">
-      <OrphaCode>2526</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2526</ExpertLink>
-      <Name lang="nl">Microcefalie - lymfoedeem - chorioretinopathie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2528</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2528</ExpertLink>
-      <Name lang="nl">Microcefalie - microcornea-syndroom, Seemanova-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <OrphaCode>2533</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2533</ExpertLink>
-      <Name lang="nl">Microcefalie - doofheid - intellectuele achterstand-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>2536</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2536</ExpertLink>
-      <Name lang="nl">Microcornea - glaucoom - afwezige frontale sinussen-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>261911</OrphaCode>
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-      <Name lang="nl">Partiële deletie van de korte arm van chromosoom 7-syndroom</Name>
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-      <Name lang="nl">Oculo-auriculo-vertebraal spectrum met radiale defecten</Name>
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-      <Name lang="nl">Microsferofakie - metafysaire dysplasie-syndroom</Name>
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-      <Name lang="nl">Microftalmie met lineaire huiddefecten-syndroom</Name>
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-    <Disorder id="19858">
-      <OrphaCode>261204</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261204</ExpertLink>
-      <Name lang="nl">16p11.2p12.2-microduplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2386">
-      <OrphaCode>2589</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2589</ExpertLink>
-      <Name lang="nl">Myoclonus - cerebellaire ataxie - doofheid-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19859">
-      <OrphaCode>261211</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261211</ExpertLink>
-      <Name lang="nl">16p11.2p12.2-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2385">
-      <OrphaCode>2588</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2588</ExpertLink>
-      <Name lang="nl">Syndroom van Myhre</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19856">
-      <OrphaCode>261190</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261190</ExpertLink>
-      <Name lang="nl">15q14-microdeletiesyndroom</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19857">
-      <OrphaCode>261197</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261197</ExpertLink>
-      <Name lang="nl">Proximale 16p11.2-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19870">
-      <OrphaCode>261295</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261295</ExpertLink>
-      <Name lang="nl">20p12.3-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19871">
-      <OrphaCode>261304</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261304</ExpertLink>
-      <Name lang="nl">Paternale 20q13.2q13.3-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19868">
-      <OrphaCode>261279</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261279</ExpertLink>
-      <Name lang="nl">17q23.1q23.2-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19869">
-      <OrphaCode>261290</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261290</ExpertLink>
-      <Name lang="nl">Trisomie 17p-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2396">
-      <OrphaCode>2617</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2617</ExpertLink>
-      <Name lang="nl">Microcefale primordiale dwerggroei, Montreal-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19866">
-      <OrphaCode>261265</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261265</ExpertLink>
-      <Name lang="nl">17q12-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19867">
-      <OrphaCode>261272</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261272</ExpertLink>
-      <Name lang="nl">17q12-microduplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2393">
-      <OrphaCode>2616</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2616</ExpertLink>
-      <Name lang="nl">3M-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19864">
-      <OrphaCode>261250</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261250</ExpertLink>
-      <Name lang="nl">16q24.3-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2392">
-      <OrphaCode>2613</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2613</ExpertLink>
-      <Name lang="nl">Nagel-patella-achtige nierziekte</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19865">
-      <OrphaCode>261257</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261257</ExpertLink>
-      <Name lang="nl">Distale 17p13.3-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19877">
-      <OrphaCode>261344</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261344</ExpertLink>
-      <Name lang="nl">Trisomie 1q-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19876">
-      <OrphaCode>261337</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261337</ExpertLink>
-      <Name lang="nl">Distale 22q11.2-microduplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19879">
-      <OrphaCode>261476</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261476</ExpertLink>
-      <Name lang="nl">Xp21-deletiesyndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="19878">
-      <OrphaCode>261349</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=261349</ExpertLink>
-      <Name lang="nl">2p15p16.1-microdeletiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
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-      <Name lang="nl">Acrale 'peeling skin'-syndroom</Name>
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-      <Name lang="nl">Acute necrotiserende encefalopathie in de kindertijd</Name>
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-      <Name lang="nl">COG4-CDG</Name>
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-      <Name lang="nl">Heterochrome iridocyclitis van Fuchs</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2774">
-      <OrphaCode>3098</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3098</ExpertLink>
-      <Name lang="nl">Rhizomeel syndroom, Urbach-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2765">
-      <OrphaCode>3078</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3078</ExpertLink>
-      <Name lang="nl">Ernstige X-gebonden intellectuele achterstand, Gustavson-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="2764">
-      <OrphaCode>3077</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3077</ExpertLink>
-      <Name lang="nl">X-gebonden intellectuele achterstand - psychose - macro-orchidisme-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
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-    <Disorder id="2767">
-      <OrphaCode>3080</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3080</ExpertLink>
-      <Name lang="nl">Intellectuele achterstand, Wolff-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="2766">
-      <OrphaCode>3079</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3079</ExpertLink>
-      <Name lang="nl">Intellectuele achterstand, Buenos Aires-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="2752">
-      <OrphaCode>3063</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3063</ExpertLink>
-      <Name lang="nl">X-gebonden intellectuele achterstand, Snyder-type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="2757">
-      <OrphaCode>3068</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3068</ExpertLink>
-      <Name lang="nl">Intellectuele achterstand - myopathie - kleine gestalte - endocrien defect-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="2614">
-      <OrphaCode>2886</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2886</ExpertLink>
-      <Name lang="nl">TARP-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="20215">
-      <OrphaCode>268861</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268861</ExpertLink>
-      <Name lang="nl">Primaire gekluisterde conus-syndroom</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="2613">
-      <OrphaCode>2885</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2885</ExpertLink>
-      <Name lang="nl">Piebaldisme - neurologische defecten-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-    <Disorder id="2612">
-      <OrphaCode>2884</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2884</ExpertLink>
-      <Name lang="nl">Piebaldisme</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2611">
-      <OrphaCode>2881</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2881</ExpertLink>
-      <Name lang="nl">Cutane fotosensitiviteit - letale colitis-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2610">
-      <OrphaCode>2879</OrphaCode>
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-      <Name lang="nl">Focomelie, Schinzel-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="20220">
-      <OrphaCode>268882</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268882</ExpertLink>
-      <Name lang="nl">Malformatie van Arnold-Chiari type I</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2620">
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-        <AverageAgeOfOnset id="23515">
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-    <Disorder id="2619">
-      <OrphaCode>2891</OrphaCode>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2617">
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>268865</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268865</ExpertLink>
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-          <Name lang="nl">Neonataal</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Geïsoleerde amyelie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2598">
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-      <Name lang="nl">Kleine gestalte - pterygium colli - hartziekte-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
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-      <Name lang="nl">Kleine gestalte - doofheid - neutrofieldisfunctie - dysmorfie-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2596">
-      <OrphaCode>2863</OrphaCode>
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-    <Disorder id="20193">
-      <OrphaCode>268744</OrphaCode>
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-      <Name lang="nl">Spina bifida cystica</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-    <Disorder id="2606">
-      <OrphaCode>2875</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2875</ExpertLink>
-      <Name lang="nl">Phakomatosis pigmentovascularis</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="20207">
-      <OrphaCode>268823</OrphaCode>
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-      <Name lang="nl">Occipitale encefalocele</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <OrphaCode>2876</OrphaCode>
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-      <Name lang="nl">PHAVER-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20206">
-      <OrphaCode>268820</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268820</ExpertLink>
-      <Name lang="nl">Craniale meningocele</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2605">
-      <OrphaCode>2874</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2874</ExpertLink>
-      <Name lang="nl">Phakomatosis pigmentokeratotica</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20204">
-      <OrphaCode>268813</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268813</ExpertLink>
-      <Name lang="nl">Myelocystocele</Name>
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-      <OrphaCode>268810</OrphaCode>
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-      <Name lang="nl">Geïsoleerde posterieure meningocele</Name>
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-      <Name lang="nl">Syndroom van Pfeiffer-Palm-Teller</Name>
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-      <Name lang="nl">Syndroom van Fuhrmann</Name>
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-      <OrphaCode>708</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=708</ExpertLink>
-      <Name lang="nl">Peters-anomalie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268363</ExpertLink>
-      <Name lang="nl">Open iniencefalie</Name>
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-    <Disorder id="20185">
-      <OrphaCode>268366</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268366</ExpertLink>
-      <Name lang="nl">Gesloten iniencefalie</Name>
-      <DisorderType id="21450">
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-    <Disorder id="2584">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2850</ExpertLink>
-      <Name lang="nl">Alopecie - intellectuele achterstand-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20186">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268369</ExpertLink>
-      <Name lang="nl">Spina bifida aperta</Name>
-      <DisorderType id="21436">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20165">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268114</ExpertLink>
-      <Name lang="nl">RAS-geassocieerde auto-immune leukoproliferatieve ziekte</Name>
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-        <AverageAgeOfOnset id="23522">
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-    <Disorder id="2564">
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-      <Name lang="nl">PARC-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268139</ExpertLink>
-      <Name lang="nl">Intraoculair medullo-epithelioom</Name>
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-      <Name lang="nl">'Spheroid body'-myopathie</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="2569">
-      <OrphaCode>2832</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2832</ExpertLink>
-      <Name lang="nl">Korte tarsus - afwezigheid van onderste wimpers-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20168">
-      <OrphaCode>268145</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268145</ExpertLink>
-      <Name lang="nl">Klassieke maple syrup urine disease</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20171">
-      <OrphaCode>268184</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268184</ExpertLink>
-      <Name lang="nl">Thiamineresponsieve maple syrup urine disease</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2570">
-      <OrphaCode>2833</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2833</ExpertLink>
-      <Name lang="nl">Stijve huid-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2571">
-      <OrphaCode>2834</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2834</ExpertLink>
-      <Name lang="nl">Rimpelige huid-syndroom</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20170">
-      <OrphaCode>268173</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268173</ExpertLink>
-      <Name lang="nl">Intermitterende maple syrup urine disease</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="2675">
-      <OrphaCode>2969</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2969</ExpertLink>
-      <Name lang="nl">Proteus-achtig syndroom</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="2674">
-      <OrphaCode>2964</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2964</ExpertLink>
-      <Name lang="nl">Autosomaal dominante prognathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2673">
-      <OrphaCode>2962</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2962</ExpertLink>
-      <Name lang="nl">Syndroom van De Barsy</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2679">
-      <OrphaCode>2973</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2973</ExpertLink>
-      <Name lang="nl">46,XX-geslachtsontwikkelingsstoornis - anorectale anomalieën-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="2678">
-      <OrphaCode>2972</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2972</ExpertLink>
-      <Name lang="nl">Niet doorkomen van tanden - hypoplasie van maxilla - genu valgum-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23487">
-          <Name lang="nl">No data available</Name>
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-    <Disorder id="2676">
-      <OrphaCode>750</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=750</ExpertLink>
-      <Name lang="nl">Pseudoachondroplasie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2682">
-      <OrphaCode>2976</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2976</ExpertLink>
-      <Name lang="nl">Pseudoleprechaunismesyndroom, Patterson-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2681">
-      <OrphaCode>2975</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2975</ExpertLink>
-      <Name lang="nl">46,XX-geslachtsontwikkelingsstoornis - skeletanomalieën-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">No data available</Name>
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-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="2686">
-      <OrphaCode>2980</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2980</ExpertLink>
-      <Name lang="nl">Acro-oto-oculair syndroom</Name>
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-    <Disorder id="2684">
-      <OrphaCode>2978</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2978</ExpertLink>
-      <Name lang="nl">Chronische intestinale pseudo-obstructie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="2659">
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-      <Name lang="nl">Brachydactylie - lange duim</Name>
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-      <OrphaCode>1848</OrphaCode>
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-      <Name lang="nl">Agenesie van nier, bilateraal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2951</ExpertLink>
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-      <Name lang="nl">Trifalangeale duimen - brachyectrodactylie-syndroom</Name>
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-    <Disorder id="20132">
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-      <Name lang="nl">Interstitiële longziekte gerelateerd aan medicatie of radiatie</Name>
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-      <DisorderType id="21401">
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-      <Name lang="nl">Syndroom van Oliver</Name>
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-      <Name lang="nl">Preaxiale polydactylie - coloboom - intellectuele achterstand-syndroom</Name>
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-      <Name lang="nl">Congenitale chylothorax</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3374</ExpertLink>
-      <Name lang="nl">Unilaterale oculaire duplicatie</Name>
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-      <Name lang="nl">Pulmonale arteriële hypertensie geassocieerd met HIV-infectie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2954">
-      <OrphaCode>3329</OrphaCode>
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-      <Name lang="nl">Aplasie van tibia - ectrodactylie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2953">
-      <OrphaCode>3328</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3328</ExpertLink>
-      <Name lang="nl">Afwezige tibia - polydactylie - arachnoïdale cyste-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="2952">
-      <OrphaCode>3327</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3327</ExpertLink>
-      <Name lang="nl">Thyrocerebrorenaal syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2951">
-      <OrphaCode>3326</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3326</ExpertLink>
-      <Name lang="nl">Dysplasie van thymus-nier-anus-long</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="2949">
-      <OrphaCode>3322</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3322</ExpertLink>
-      <Name lang="nl">Syndroom van Hoyeraal-Hreidarsson</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="2947">
-      <OrphaCode>3317</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3317</ExpertLink>
-      <Name lang="nl">Thoracolaryngopelviene dysplasie</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2946">
-      <OrphaCode>3316</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3316</ExpertLink>
-      <Name lang="nl">Syndroom van Thomas</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2945">
-      <OrphaCode>3314</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3314</ExpertLink>
-      <Name lang="nl">Ziekte van Thiemann, familiale vorm</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2974">
-      <OrphaCode>3355</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3355</ExpertLink>
-      <Name lang="nl">Tricho-odonto-onychiale dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="20319">
-      <OrphaCode>275555</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=275555</ExpertLink>
-      <Name lang="nl">Pre-eclampsie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-      <OrphaCode>275543</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=275543</ExpertLink>
-      <Name lang="nl">L1-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-      <OrphaCode>3353</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3353</ExpertLink>
-      <Name lang="nl">Trichodermodysplasie - dentale veranderingen-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Auto-immune lymfoproliferatieve ziekte van Dianzani</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Auto-immuun lymfoproliferatief syndroom-recidiverende virale infecties door CASP8-deficiëntie</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <OrphaCode>2460</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2460</ExpertLink>
-      <Name lang="nl">Syndroom van Van den Ende-Gupta</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20226">
-      <OrphaCode>268940</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268940</ExpertLink>
-      <Name lang="nl">Bilaterale polymicrogyrie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20227">
-      <OrphaCode>268943</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268943</ExpertLink>
-      <Name lang="nl">Unilaterale polymicrogyrie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3010">
-      <OrphaCode>3416</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3416</ExpertLink>
-      <Name lang="nl">Hyperostosis corticalis generalisata</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20225">
-      <OrphaCode>268936</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268936</ExpertLink>
-      <Name lang="nl">Geïsoleerde arhinencefalie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20228">
-      <OrphaCode>268947</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=268947</ExpertLink>
-      <Name lang="nl">Unilaterale focale polymicrogyrie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3012">
-      <OrphaCode>3417</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3417</ExpertLink>
-      <Name lang="nl">Syndroom van Van den Bosch</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20251">
-      <OrphaCode>269229</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269229</ExpertLink>
-      <Name lang="nl">Pontiene tegmentale kap-dysplasie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3035">
-      <OrphaCode>3453</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3453</ExpertLink>
-      <Name lang="nl">Auto-immune polyendocrinopathie type 1</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3032">
-      <OrphaCode>3448</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3448</ExpertLink>
-      <Name lang="nl">Weaver-Williamssyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20249">
-      <OrphaCode>269221</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269221</ExpertLink>
-      <Name lang="nl">Geïsoleerde bilaterale hypoplasie van cerebellaire hemisfeer</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3033">
-      <OrphaCode>3449</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3449</ExpertLink>
-      <Name lang="nl">Syndroom van Weill-Marchesani</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="20248">
-      <OrphaCode>269218</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269218</ExpertLink>
-      <Name lang="nl">Geïsoleerde unilaterale hypoplasie van cerebellaire hemisfeer</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3038">
-      <OrphaCode>3456</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3456</ExpertLink>
-      <Name lang="nl">Syndroom van Wildervanck</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20253">
-      <OrphaCode>269510</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269510</ExpertLink>
-      <Name lang="nl">Congenitale niet-communicerende hydrocefalus</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="3036">
-      <OrphaCode>3454</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3454</ExpertLink>
-      <Name lang="nl">Syndroom van Wieacker-Wolff</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="3037">
-      <OrphaCode>3455</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3455</ExpertLink>
-      <Name lang="nl">Syndroom van Wiedemann-Rautenstrauch</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="20252">
-      <OrphaCode>269505</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269505</ExpertLink>
-      <Name lang="nl">Congenitale communicerende hydrocefalus</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20243">
-      <OrphaCode>269203</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269203</ExpertLink>
-      <Name lang="nl">Geïsoleerde cerebellaire vermis-agenesie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20241">
-      <OrphaCode>269197</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269197</ExpertLink>
-      <Name lang="nl">Glio-ependymale/ependymale cyste</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="3024">
-      <OrphaCode>3434</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3434</ExpertLink>
-      <Name lang="nl">MMEP-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="20247">
-      <OrphaCode>269215</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=269215</ExpertLink>
-      <Name lang="nl">Geïsoleerde Dandy-Walker malformatie zonder hydrocefalus</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <TypeOfInheritance id="23424">
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-      <OrphaCode>1856</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1856</ExpertLink>
-      <Name lang="nl">Spondyloperifere dysplasie - korte ulna-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="20453">
-      <OrphaCode>280315</OrphaCode>
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-      <Name lang="nl">Auto-immune pancreatitis type 2</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="2853">
-      <OrphaCode>3181</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3181</ExpertLink>
-      <Name lang="nl">Deformiteit van Sprengel</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20452">
-      <OrphaCode>280302</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280302</ExpertLink>
-      <Name lang="nl">Auto-immune pancreatitis type 1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="20455">
-      <OrphaCode>280333</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280333</ExpertLink>
-      <Name lang="nl">Alfa-dystroglycaan-gerelateerde limb-girdle-spierdystrofie R16</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="20454">
-      <OrphaCode>280325</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280325</ExpertLink>
-      <Name lang="nl">Distale deletie 12p-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20449">
-      <OrphaCode>280293</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280293</ExpertLink>
-      <Name lang="nl">Pelizaeus-Merzbacher-achtige ziekte door AIMP1-mutatie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="20448">
-      <OrphaCode>280288</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280288</ExpertLink>
-      <Name lang="nl">Pelizaeus-Merzbacher-achtige ziekte door HSPD1-mutatie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2860">
-      <OrphaCode>3194</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3194</ExpertLink>
-      <Name lang="nl">Corneodermato-ossaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="20460">
-      <OrphaCode>280365</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280365</ExpertLink>
-      <Name lang="nl">Autosomaal semidominante ernstige lipodystrofische laminopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23466">
-          <Name lang="nl">Semi-dominant</Name>
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-    <Disorder id="20463">
-      <OrphaCode>280379</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280379</ExpertLink>
-      <Name lang="nl">Erytropoëtische uroporfyrie geassocieerd met myeloïde maligniteiten</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2862">
-      <OrphaCode>3197</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3197</ExpertLink>
-      <Name lang="nl">Erfelijke hyperekplexie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2863">
-      <OrphaCode>3199</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3199</ExpertLink>
-      <Name lang="nl">Syndroom van Stimmler</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2856">
-      <OrphaCode>3184</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3184</ExpertLink>
-      <Name lang="nl">Steatocystoma multiplex - natale tanden-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>3186</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3186</ExpertLink>
-      <Name lang="nl">Holoprosencefalie - radiale, cardiale en renale anomalieën-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">PLIN1-gerelateerde familiale partiële lipodystrofie</Name>
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-      <Name lang="nl">Syndroom van Senior-Loken</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280071</ExpertLink>
-      <Name lang="nl">ALG11-CDG</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3157</ExpertLink>
-      <Name lang="nl">Septo-optische dysplasie-spectrum</Name>
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-      <OrphaCode>280210</OrphaCode>
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-      <Name lang="nl">Ziekte van Pelizaeus-Merzbacher, connatale vorm</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <Name lang="nl">Ziekte van Pelizaeus-Merzbacher, klassieke vorm</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280200</ExpertLink>
-      <Name lang="nl">Microforme holoprosencefalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20384">
-      <OrphaCode>276575</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276575</ExpertLink>
-      <Name lang="nl">Autosomaal dominant hyperinsulinisme door SUR1-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="20387">
-      <OrphaCode>276598</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276598</ExpertLink>
-      <Name lang="nl">Diazoxideresistent focaal hyperinsulinisme door SUR1-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="2914">
-      <OrphaCode>3262</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3262</ExpertLink>
-      <Name lang="nl">Syndroom van Dobrow</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20389">
-      <OrphaCode>276608</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276608</ExpertLink>
-      <Name lang="nl">Niet-insulinoom pancreatogeen hypoglycemisch syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2916">
-      <OrphaCode>3265</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3265</ExpertLink>
-      <Name lang="nl">Geïsoleerde humeroradiale synostose</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="20388">
-      <OrphaCode>276603</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276603</ExpertLink>
-      <Name lang="nl">Diazoxideresistent focaal hyperinsulinisme door Kir6.2-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2917">
-      <OrphaCode>3266</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3266</ExpertLink>
-      <Name lang="nl">Geïsoleerde humeroradio-ulnaire synostose</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="20390">
-      <OrphaCode>276621</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276621</ExpertLink>
-      <Name lang="nl">Sporadisch feochromocytoom/secreterend paraganglioom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2919">
-      <OrphaCode>3268</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3268</ExpertLink>
-      <Name lang="nl">Radio-ulnaire synostose - microcefalie - scoliose-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="20393">
-      <OrphaCode>276630</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276630</ExpertLink>
-      <Name lang="nl">Symptomatische vorm van Coffin-Lowrysyndroom bij vrouwelijke dragers</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-      <OrphaCode>3270</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3270</ExpertLink>
-      <Name lang="nl">Radio-ulnaire synostose - ontwikkelingsachterstand - hypotonie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="2923">
-      <OrphaCode>3275</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3275</ExpertLink>
-      <Name lang="nl">Spondylocarpotarsale synostose</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="2927">
-      <OrphaCode>425</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=425</ExpertLink>
-      <Name lang="nl">Apolipoproteïne A-I-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>3291</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3291</ExpertLink>
-      <Name lang="nl">Syndroom van Teebi-Shaltout</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="2933">
-      <OrphaCode>3293</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3293</ExpertLink>
-      <Name lang="nl">Telecanthus - hypertelorisme - strabisme - pes cavus-syndroom</Name>
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-        <TypeOfInheritance id="23480">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3292</ExpertLink>
-      <Name lang="nl">Camptodactylie-syndroom van Tel Hashomer</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
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-      <OrphaCode>279882</OrphaCode>
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-        <TypeOfInheritance id="23480">
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-      <Name lang="nl">Anomalieën van extensorpezen van vinger</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=279894</ExpertLink>
-      <Name lang="nl">Toxische maculopathie door antimalariamiddel</Name>
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-      <Name lang="nl">Tetra-amelie - multipele malformaties-syndroom</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
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-    </Disorder>
-    <Disorder id="20411">
-      <OrphaCode>279897</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=279897</ExpertLink>
-      <Name lang="nl">Primair oculocerebraal lymfoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="20412">
-      <OrphaCode>279904</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=279904</ExpertLink>
-      <Name lang="nl">Primair intraoculair lymfoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="2940">
-      <OrphaCode>3304</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3304</ExpertLink>
-      <Name lang="nl">Tetralogie van Fallot - intellectuele achterstand - groeiachterstand-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="2943">
-      <OrphaCode>3312</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3312</ExpertLink>
-      <Name lang="nl">Thalidomide-embryopathie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="20414">
-      <OrphaCode>279914</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=279914</ExpertLink>
-      <Name lang="nl">Intermediaire uveïtis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="20415">
-      <OrphaCode>279919</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=279919</ExpertLink>
-      <Name lang="nl">Infectieuze posterieure uveïtis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="20355">
-      <OrphaCode>276198</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276198</ExpertLink>
-      <Name lang="nl">Spinocerebellaire ataxie type 36</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2882">
-      <OrphaCode>3225</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3225</ExpertLink>
-      <Name lang="nl">Gehoorverlies - familiale insensitiviteit van speekselklier voor aldosteron-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="20354">
-      <OrphaCode>276193</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276193</ExpertLink>
-      <Name lang="nl">Spinocerebellaire ataxie type 35</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="20353">
-      <OrphaCode>276183</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276183</ExpertLink>
-      <Name lang="nl">Spinocerebellaire ataxie type 32</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="2881">
-      <OrphaCode>3224</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3224</ExpertLink>
-      <Name lang="nl">Doofheid - genitale anomalieën - metacarpale en metatarsale synostose-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="20352">
-      <OrphaCode>276174</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276174</ExpertLink>
-      <Name lang="nl">Idiopathische recidiverende stupor</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="20359">
-      <OrphaCode>276238</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276238</ExpertLink>
-      <Name lang="nl">Ziekte van Machado-Joseph type 1</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="20358">
-      <OrphaCode>276234</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276234</ExpertLink>
-      <Name lang="nl">Niet-syndromale mannelijke onvruchtbaarheid als gevolg van een spermamotiliteitsstoornis</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="20357">
-      <OrphaCode>276223</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276223</ExpertLink>
-      <Name lang="nl">Mucopolysacharidose type 6, traag progressief</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
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-    <Disorder id="20356">
-      <OrphaCode>276212</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276212</ExpertLink>
-      <Name lang="nl">Mucopolysacharidose type 6, snel progressief</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="2890">
-      <OrphaCode>3230</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3230</ExpertLink>
-      <Name lang="nl">Doofheid - oligodontie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
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-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Doofheid - onychodystrofie-syndroom</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-        <AverageAgeOfOnset id="23529">
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-        <TypeOfInheritance id="23410">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="20361">
-      <OrphaCode>276244</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=276244</ExpertLink>
-      <Name lang="nl">Ziekte van Machado-Joseph type 3</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="20360">
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-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
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-        <TypeOfInheritance id="23410">
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-      <Name lang="nl">Progressieve doofheid met stijgbeugelfixatie</Name>
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-      <DisorderGroup id="36547">
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-        <AverageAgeOfOnset id="23529">
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="2895">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3236</ExpertLink>
-      <Name lang="nl">Conductieve doofheid - ptosis - skeletanomalieën-syndroom</Name>
-      <DisorderType id="21401">
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="2892">
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-        <AverageAgeOfOnset id="23515">
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="2893">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3233</ExpertLink>
-      <Name lang="nl">Cochleosacculaire degeneratie - cataract-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
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-      <Name lang="nl">Cardiospondylocarpofaciaal syndroom</Name>
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-      <Name lang="nl">Symfalangisme met meervoudige anomalieën van handen en voeten</Name>
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-      <Name lang="nl">10q22.3q23.3-microdeletiesyndroom</Name>
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-      <Name lang="nl">Maligne niet-dysgerminomateuze kiemceltumor van ovarium</Name>
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-      <OrphaCode>206549</OrphaCode>
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-    <Disorder id="18523">
-      <OrphaCode>206564</OrphaCode>
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-      <Name lang="nl">POMT2-gerelateerde limb-girdle-spierdystrofie R14</Name>
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-      <Name lang="nl">Autosomaal recessieve lage motorneuronziekte met aanvang in de kindertijd</Name>
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-      <Name lang="nl">Bilaterale gegeneraliseerde polymicrogyrie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-    <Disorder id="3183">
-      <OrphaCode>3051</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3051</ExpertLink>
-      <Name lang="nl">Syndroom van Nicolaides-Baraitser</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="18605">
-      <OrphaCode>208444</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=208444</ExpertLink>
-      <Name lang="nl">Bilaterale frontale polymicrogyrie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="18604">
-      <OrphaCode>208441</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=208441</ExpertLink>
-      <Name lang="nl">Bilaterale parasagittale parieto-occipitale polymicrogyrie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="3181">
-      <OrphaCode>1134</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1134</ExpertLink>
-      <Name lang="nl">Geïsoleerde arrhinie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="3174">
-      <OrphaCode>1768</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1768</ExpertLink>
-      <Name lang="nl">Familiale caudale dysgenesie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="3175">
-      <OrphaCode>2204</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2204</ExpertLink>
-      <Name lang="nl">Dysplastische corticale hyperostose, Kozlowski-Tsuruta-type</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-    <Disorder id="3173">
-      <OrphaCode>2963</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2963</ExpertLink>
-      <Name lang="nl">Progeroïd syndroom, Petty-type</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-      <OrphaCode>2619</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2619</ExpertLink>
-      <Name lang="nl">Brachydactyleuze dwerggroei, Mseleni-type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="3169">
-      <OrphaCode>1541</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1541</ExpertLink>
-      <Name lang="nl">Craniosynostose, Boston-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="3096">
-      <OrphaCode>1415</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1415</ExpertLink>
-      <Name lang="nl">Syndroom van Hardikar</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="3101">
-      <OrphaCode>2151</OrphaCode>
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-      <Name lang="nl">Ziekte van Hirschsprung - ganglioneuroblastoom-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="18654">
-      <OrphaCode>209335</OrphaCode>
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-      <Name lang="nl">Autosomaal dominante proximale spinale musculaire atrofie met aanvang bij volwassenen</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="18655">
-      <OrphaCode>209341</OrphaCode>
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-      <Name lang="nl">DYNC1H1-gerelateerde autosomaal dominante proximale spinale musculaire atrofie met aanvang in de kindertijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1884</ExpertLink>
-      <Name lang="nl">Ectopia lentis - chorioretinale dystrofie - myopie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="18680">
-      <OrphaCode>209981</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209981</ExpertLink>
-      <Name lang="nl">IRIDA-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="3128">
-      <OrphaCode>1459</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1459</ExpertLink>
-      <Name lang="nl">Coeliakie - epilepsie - cerebrale calcificatie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="18686">
-      <OrphaCode>210133</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=210133</ExpertLink>
-      <Name lang="nl">Leukonychia totalis - acanthosis-nigricans-achtige laesies - abnormaal haar-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="18687">
-      <OrphaCode>210136</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=210136</ExpertLink>
-      <Name lang="nl">Longfibrose - leverhyperplasie - beenmerghypoplasie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3134">
-      <OrphaCode>2582</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2582</ExpertLink>
-      <Name lang="nl">Myalgie - eosinofilie-syndroom geassocieerd met tryptofaan</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="18684">
-      <OrphaCode>210122</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=210122</ExpertLink>
-      <Name lang="nl">Congenitale alveolaire capillaire dysplasie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18685">
-      <OrphaCode>210128</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=210128</ExpertLink>
-      <Name lang="nl">Urocaanzuuracidurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="3132">
-      <OrphaCode>2254</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2254</ExpertLink>
-      <Name lang="nl">Pontocerebellaire hypoplasie type 1</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="18674">
-      <OrphaCode>209959</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209959</ExpertLink>
-      <Name lang="nl">Faco-anafylactische uveïtis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18675">
-      <OrphaCode>209964</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209964</ExpertLink>
-      <Name lang="nl">Solitaire rectale ulcus-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18672">
-      <OrphaCode>209951</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209951</ExpertLink>
-      <Name lang="nl">Autosomale spastische paraplegie type 18</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="18673">
-      <OrphaCode>209956</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209956</ExpertLink>
-      <Name lang="nl">Idiopathische uveale effusie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
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-    <Disorder id="18678">
-      <OrphaCode>209973</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209973</ExpertLink>
-      <Name lang="nl">Benigne nachtelijke alternerende hemiplegie op kinderleeftijd</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="18676">
-      <OrphaCode>209967</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209967</ExpertLink>
-      <Name lang="nl">Episodische ataxie type 6</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="18677">
-      <OrphaCode>209970</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209970</ExpertLink>
-      <Name lang="nl">Episodische ataxie type 7</Name>
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-      </DisorderType>
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-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="3114">
-      <OrphaCode>2795</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2795</ExpertLink>
-      <Name lang="nl">Polycystische ovaria - urethrale sfincterdisfunctie-syndroom</Name>
-      <DisorderType id="21394">
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-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="18667">
-      <OrphaCode>209908</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209908</ExpertLink>
-      <Name lang="nl">Geïsoleerde spraakapraxie op kinderleeftijd</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
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-    <Disorder id="18666">
-      <OrphaCode>209905</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209905</ExpertLink>
-      <Name lang="nl">Hersenen - long - schildklier-syndroom</Name>
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-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="18665">
-      <OrphaCode>209902</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209902</ExpertLink>
-      <Name lang="nl">Hypercholesterolemie door deficiëntie van cholesterol-7-alfa-hydroxylase</Name>
-      <DisorderType id="21394">
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <OrphaCode>2666</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2666</ExpertLink>
-      <Name lang="nl">Volwassen familiale nefronoftise - spastische quadriparese-syndroom</Name>
-      <DisorderType id="21394">
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="18671">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209943</ExpertLink>
-      <Name lang="nl">IRVAN-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23494">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=209932</ExpertLink>
-      <Name lang="nl">Kegeldystrofie met supernormale staafrespons</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <Name lang="nl">Congenitaal niet-gecorrigeerde transpositie van grote slagaders met hartmalformatie</Name>
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-      <Name lang="nl">Dubbele uterus - hemivagina - renale agenesie-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=882</ExpertLink>
-      <Name lang="nl">Tyrosinemie type 1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <Name lang="nl">Ziekte van Von Willebrand</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3508">
-      <OrphaCode>1787</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1787</ExpertLink>
-      <Name lang="nl">Acrofaciale dysostose, Palagonia-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18804">
-      <OrphaCode>216981</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=216981</ExpertLink>
-      <Name lang="nl">Ziekte van Niemann-Pick type C, juveniele neurologische aanvang</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18807">
-      <OrphaCode>217008</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217008</ExpertLink>
-      <Name lang="nl">Syndroom van Bockenheimer</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18809">
-      <OrphaCode>217017</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217017</ExpertLink>
-      <Name lang="nl">Syndroom van Zechi-Ceide</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18808">
-      <OrphaCode>217012</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217012</ExpertLink>
-      <Name lang="nl">Spinocerebellaire ataxie type 31</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3513">
-      <OrphaCode>2088</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2088</ExpertLink>
-      <Name lang="nl">Syndroom van Fanconi-Bickel</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18811">
-      <OrphaCode>217026</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217026</ExpertLink>
-      <Name lang="nl">Microcefalie - faciocardioskeletaal syndroom, Hadziselimovic-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18829">
-      <OrphaCode>217266</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217266</ExpertLink>
-      <Name lang="nl">BNAR-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3404">
-      <OrphaCode>179</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=179</ExpertLink>
-      <Name lang="nl">Chorioretinopathie, Birdshot-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18828">
-      <OrphaCode>217260</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217260</ExpertLink>
-      <Name lang="nl">Progressieve multifocale leuko-encefalopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3402">
-      <OrphaCode>292</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=292</ExpertLink>
-      <Name lang="nl">Congenitale infectie door enterovirus</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18827">
-      <OrphaCode>217253</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217253</ExpertLink>
-      <Name lang="nl">NMDA-receptor-encefalitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3403">
-      <OrphaCode>767</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=767</ExpertLink>
-      <Name lang="nl">Polyarteriitis nodosa</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3400">
-      <OrphaCode>2584</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2584</ExpertLink>
-      <Name lang="nl">Klassieke mycosis fungoides</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18825">
-      <OrphaCode>217093</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217093</ExpertLink>
-      <Name lang="nl">Mucopolysacharidose type 2, geattenueerde vorm</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3401">
-      <OrphaCode>3162</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3162</ExpertLink>
-      <Name lang="nl">Syndroom van Sézary</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18824">
-      <OrphaCode>217085</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217085</ExpertLink>
-      <Name lang="nl">Mucopolysacharidose type 2, ernstige vorm</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18823">
-      <OrphaCode>217080</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217080</ExpertLink>
-      <Name lang="nl">Pulmonale fungale infecties bij risicopatiënten</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18822">
-      <OrphaCode>217074</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217074</ExpertLink>
-      <Name lang="nl">Zeldzaam carcinoom van pancreas</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3399">
-      <OrphaCode>2330</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2330</ExpertLink>
-      <Name lang="nl">Fenomeen van Kasabach-Merritt</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18821">
-      <OrphaCode>217071</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217071</ExpertLink>
-      <Name lang="nl">Niercelcarcinoom</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="18820">
-      <OrphaCode>217067</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217067</ExpertLink>
-      <Name lang="nl">Pouchitis</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
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-      <Name lang="nl">Geïsoleerde horlogeglasnagel</Name>
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-      <OrphaCode>217055</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217055</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve intermediaire ziekte van Charcot-Marie-Tooth type A</Name>
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-      <Name lang="nl">RIN2-syndroom</Name>
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-      <OrphaCode>1686</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1686</ExpertLink>
-      <Name lang="nl">Cardiaal divertikel</Name>
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-    <Disorder id="18863">
-      <OrphaCode>217566</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217566</ExpertLink>
-      <Name lang="nl">Chronische ademhalingsnood met deficiëntie van surfactantmetabolisme</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="18862">
-      <OrphaCode>217563</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217563</ExpertLink>
-      <Name lang="nl">Neonataal acuut ademhalingsnoodsyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>217407</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217407</ExpertLink>
-      <Name lang="nl">Hereditaire hypotrichose met recidiverende huidblaasjes</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="3434">
-      <OrphaCode>1456</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1456</ExpertLink>
-      <Name lang="nl">Mid-aorta syndroom</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="18859">
-      <OrphaCode>217467</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217467</ExpertLink>
-      <Name lang="nl">Erfelijke trombofilie als gevolg van congenitale histidine-rijke (poly-L) glycoproteïnedeficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <OrphaCode>1457</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1457</ExpertLink>
-      <Name lang="nl">Aortacoarctatie</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-      <OrphaCode>217390</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217390</ExpertLink>
-      <Name lang="nl">Gecombineerde immuundeficiëntie als gevolg van DOCK8-deficiëntie</Name>
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-      <OrphaCode>1132</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1132</ExpertLink>
-      <Name lang="nl">Aortaboogdefecten</Name>
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-        <Name lang="nl">Categorie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217385</ExpertLink>
-      <Name lang="nl">17p13.3-microduplicatiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="18855">
-      <OrphaCode>217399</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217399</ExpertLink>
-      <Name lang="nl">Congenitale ongevoeligheid voor pijn - hyperhidrose - afwezigheid van sensorische innervatie van huid</Name>
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-      <OrphaCode>217396</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217396</ExpertLink>
-      <Name lang="nl">Progressieve polyneuropathie met bilaterale striatale necrose</Name>
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-      <OrphaCode>982</OrphaCode>
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-      <Name lang="nl">Agenesie van pulmonalisklep</Name>
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-      <Name lang="nl">Acuut infantiel leverfalen door synthesedefect van mtDNA-gecodeerde proteïnen</Name>
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-      <Name lang="nl">19q13.11-microdeletiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217382</ExpertLink>
-      <Name lang="nl">Neurodegeneratief syndroom door deficiëntie van cerebraal folaattransport</Name>
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-      <Name lang="nl">Aneurysma van sinus van Valsalva</Name>
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-    <Disorder id="3448">
-      <OrphaCode>2299</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2299</ExpertLink>
-      <Name lang="nl">Aortaboogonderbreking</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3451">
-      <OrphaCode>3427</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3427</ExpertLink>
-      <Name lang="nl">Linkerventrikel met dubbele uitstroom</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3450">
-      <OrphaCode>3426</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3426</ExpertLink>
-      <Name lang="nl">Rechterventrikel met dubbele uitstroom</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3445">
-      <OrphaCode>439</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439</ExpertLink>
-      <Name lang="nl">Geïsoleerde rechterventrikelhypoplasie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3444">
-      <OrphaCode>422</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=422</ExpertLink>
-      <Name lang="nl">Idiopathische/erfelijke pulmonale arteriële hypertensie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="3">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3441">
-      <OrphaCode>2038</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2038</ExpertLink>
-      <Name lang="nl">Pulmonale arterioveneuze malformatie</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3443">
-      <OrphaCode>2041</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2041</ExpertLink>
-      <Name lang="nl">Coronaire arteriële fistel</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3338">
-      <OrphaCode>282</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=282</ExpertLink>
-      <Name lang="nl">Frontotemporale dementie</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3336">
-      <OrphaCode>331</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=331</ExpertLink>
-      <Name lang="nl">Congenitale factor XIII-deficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3343">
-      <OrphaCode>159</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=159</ExpertLink>
-      <Name lang="nl">Deficiëntie van carnitine-acylcarnitine translocase</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3341">
-      <OrphaCode>707</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=707</ExpertLink>
-      <Name lang="nl">Pest</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3331">
-      <OrphaCode>335</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=335</ExpertLink>
-      <Name lang="nl">Congenitale deficiëntie van fibrinogeen</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="3335">
-      <OrphaCode>79</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79</ExpertLink>
-      <Name lang="nl">Congenitale deficiëntie van alfa2-antiplasmine</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="18885">
-      <OrphaCode>217656</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=217656</ExpertLink>
-      <Name lang="nl">Erfelijke geïsoleerde aritmogene cardiomyopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="3332">
-      <OrphaCode>1070</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1070</ExpertLink>
-      <Name lang="nl">Anisakiasis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="3333">
-      <OrphaCode>1467</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1467</ExpertLink>
-      <Name lang="nl">Syndroom van Cogan</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="3355">
-      <OrphaCode>2157</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2157</ExpertLink>
-      <Name lang="nl">Histidinemie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="18906">
-      <OrphaCode>220402</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220402</ExpertLink>
-      <Name lang="nl">Gelimiteerde cutane systemische sclerose</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="3354">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3124</ExpertLink>
-      <Name lang="nl">Saccharopinurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="18907">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220407</ExpertLink>
-      <Name lang="nl">Gelimiteerde systemische sclerose</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220386</ExpertLink>
-      <Name lang="nl">Semilobaire holoprosencefalie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23424">
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="3353">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2203</ExpertLink>
-      <Name lang="nl">Hyperlysinemie</Name>
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-        <TypeOfInheritance id="23417">
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-      <OrphaCode>220393</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220393</ExpertLink>
-      <Name lang="nl">Diffuse cutane systemische sclerose</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="3359">
-      <OrphaCode>332</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=332</ExpertLink>
-      <Name lang="nl">Congenitale deficiëntie van intrinsieke factor</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="18910">
-      <OrphaCode>220448</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220448</ExpertLink>
-      <Name lang="nl">Macrotrombocytopenie met mitralisklepinsufficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="3358">
-      <OrphaCode>2967</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2967</ExpertLink>
-      <Name lang="nl">Transcobalamine I-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="18908">
-      <OrphaCode>220436</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220436</ExpertLink>
-      <Name lang="nl">Quebec-bloedplaatjesstoornis</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="3356">
-      <OrphaCode>2195</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2195</ExpertLink>
-      <Name lang="nl">Dicarboxyl-aminoacidurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="3351">
-      <OrphaCode>2170</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2170</ExpertLink>
-      <Name lang="nl">Deficiëntie van methylcobalamine type cblG</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="18903">
-      <OrphaCode>220295</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220295</ExpertLink>
-      <Name lang="nl">Xeroderma pigmentosum - syndroom van Cockayne-complex</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="3349">
-      <OrphaCode>414</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=414</ExpertLink>
-      <Name lang="nl">Gyrate atrofie van choroidea en retina</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="3369">
-      <OrphaCode>622</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=622</ExpertLink>
-      <Name lang="nl">Homocystinurie zonder methylmalonacidurie</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="3370">
-      <OrphaCode>927</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=927</ExpertLink>
-      <Name lang="nl">Hyperammoniëmie door deficiëntie van N-acetylglutamaatsynthetase</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="3372">
-      <OrphaCode>3402</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3402</ExpertLink>
-      <Name lang="nl">Voorbijgaande tyrosinemie bij de pasgeborene</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="3374">
-      <OrphaCode>2880</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2880</ExpertLink>
-      <Name lang="nl">Deficiëntie van fosfo-enolpyruvaat-carboxykinase</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23438">
-          <Name lang="nl">Mitochondriale overerving</Name>
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-    <Disorder id="3360">
-      <OrphaCode>941</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=941</ExpertLink>
-      <Name lang="nl">D-glycerinezuuracidurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="18913">
-      <OrphaCode>220465</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220465</ExpertLink>
-      <Name lang="nl">Syndroom van Laron met immuundeficiëntie</Name>
-      <DisorderType id="21394">
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-        <AverageAgeOfOnset id="23515">
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-      <OrphaCode>220460</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220460</ExpertLink>
-      <Name lang="nl">Geattenueerde familiale adenomateuze polyposis</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=220489</ExpertLink>
-      <Name lang="nl">Zeldzame erfelijke hemochromatose</Name>
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-      <Name lang="nl">2-hydroxyglutaaracidurie</Name>
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-      <Name lang="nl">Syndroom van Joubert met renaal defect</Name>
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-      <Name lang="nl">Erfelijk syndoom van borst- en/of ovariumkanker</Name>
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-      <Name lang="nl">Prolactinoom</Name>
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-      <Name lang="nl">Trigeminusneuralgie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=538</ExpertLink>
-      <Name lang="nl">Lymfangioleiomyomatose</Name>
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-      <Name lang="nl">Glossofaryngeale neuralgie</Name>
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-      <Name lang="nl">Post-poliomyelitissyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=221120</ExpertLink>
-      <Name lang="nl">Pseudoaminopterinesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=221126</ExpertLink>
-      <Name lang="nl">Vasculopathie van Fowler</Name>
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-      <Name lang="nl">Gecombineerde immuundeficiëntie met facio-oculoskeletale anomalieën</Name>
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-      <Name lang="nl">Confetti-achtige macula-atrofie</Name>
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-      <Name lang="nl">Idiopathische CD4-lymfocytopenie</Name>
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-      <OrphaCode>389</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=389</ExpertLink>
-      <Name lang="nl">Langerhanscelhistiocytose</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>228012</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228012</ExpertLink>
-      <Name lang="nl">Progressief sensorineuraal gehoorverlies - hypertrofische cardiomyopathie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>616</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=616</ExpertLink>
-      <Name lang="nl">Medulloblastoom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="3750">
-      <OrphaCode>301</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=301</ExpertLink>
-      <Name lang="nl">Ependymale tumor</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="3749">
-      <OrphaCode>541</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=541</ExpertLink>
-      <Name lang="nl">Primaire cutane CD30+ T-cel lymfoproliferatieve ziekte</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="3747">
-      <OrphaCode>543</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=543</ExpertLink>
-      <Name lang="nl">Burkitt-lymfoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="3759">
-      <OrphaCode>319</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319</ExpertLink>
-      <Name lang="nl">Skeletaal Ewing-sarcoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="19054">
-      <OrphaCode>227535</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=227535</ExpertLink>
-      <Name lang="nl">Erfelijke borstkanker</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-      <OrphaCode>668</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=668</ExpertLink>
-      <Name lang="nl">Osteosarcoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="19053">
-      <OrphaCode>227510</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=227510</ExpertLink>
-      <Name lang="nl">Meervoudige systeematrofie, cerebellair type</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="3754">
-      <OrphaCode>94</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=94</ExpertLink>
-      <Name lang="nl">Astrocytoom</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>360</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=360</ExpertLink>
-      <Name lang="nl">Glioblastoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="19029">
-      <OrphaCode>226292</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=226292</ExpertLink>
-      <Name lang="nl">Permanente congenitale hypothyreoïdie</Name>
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-      <OrphaCode>513</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=513</ExpertLink>
-      <Name lang="nl">Acute lymfoblastische leukemie</Name>
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-      <Name lang="nl">Esthesioneuroblastoom</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="3734">
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Pseudoxanthoma elasticum</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="19035">
-      <OrphaCode>226313</OrphaCode>
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-      <OrphaCode>391</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=391</ExpertLink>
-      <Name lang="nl">Klassiek Hodgkin-lymfoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="3717">
-      <OrphaCode>2260</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2260</ExpertLink>
-      <Name lang="nl">Oligomeganefronie</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=503</ExpertLink>
-      <Name lang="nl">Syndroom van Larsen</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="3719">
-      <OrphaCode>1652</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1652</ExpertLink>
-      <Name lang="nl">Ziekte van Dent</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      <OrphaCode>2542</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2542</ExpertLink>
-      <Name lang="nl">Geïsoleerde microftalmie - anoftalmie - coloboom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="3712">
-      <OrphaCode>3280</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3280</ExpertLink>
-      <Name lang="nl">Syringomyelie</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Megalencefalische leuko-encefalopathie met subcorticale cysten</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>3337</OrphaCode>
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-      <Name lang="nl">Primair renotubulair syndroom van Fanconi</Name>
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-      <OrphaCode>223</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=223</ExpertLink>
-      <Name lang="nl">Resistentie voor arginine-vasopressine</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <OrphaCode>757</OrphaCode>
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-      <Name lang="nl">Pseudohypoaldosteronisme type 2</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Hereditaire deficiëntie van butyrylcholinesterase</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <OrphaCode>228396</OrphaCode>
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-      <Name lang="nl">Ptosis - beperkte opwaartse oogbeweging - agenesie van punctum lacrimale-syndroom</Name>
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-      <Name lang="nl">Spondylo-megaepifysaire-metafysaire dysplasie</Name>
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-      <Name lang="nl">Frontonasale dysplasie - alopecie - genitale anomalieën-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>228410</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228410</ExpertLink>
-      <Name lang="nl">Hartanomalieën - kleine gestalte - gewrichtshypermobiliteit - faciale dysmorfie-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-      <OrphaCode>228399</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228399</ExpertLink>
-      <Name lang="nl">8q12-microduplicatiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="3700">
-      <OrphaCode>2781</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2781</ExpertLink>
-      <Name lang="nl">Osteopetrose en gerelateerde aandoeningen</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228402</ExpertLink>
-      <Name lang="nl">2q23.1-microdeletiesyndroom</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-      <OrphaCode>228363</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228363</ExpertLink>
-      <Name lang="nl">CLN6-ziekte</Name>
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-      <Name lang="nl">5q14.3-microdeletiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228379</ExpertLink>
-      <Name lang="nl">Virusgeassocieerde trichodysplasia spinulosa</Name>
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-      <Name lang="nl">Ziekte van Charcot-Marie-Tooth type 2B5</Name>
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-      <OrphaCode>228308</OrphaCode>
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-      <Name lang="nl">Auto-immune hemolytische anemie, koude-type</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228240</ExpertLink>
-      <Name lang="nl">Elastoderma</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=135</ExpertLink>
-      <Name lang="nl">CACH-syndroom</Name>
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-      <OrphaCode>228243</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228243</ExpertLink>
-      <Name lang="nl">Elastofibroma dorsi</Name>
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-      <OrphaCode>228247</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228247</ExpertLink>
-      <Name lang="nl">Verworven pseudoxanthoma elasticum</Name>
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-    <Disorder id="19091">
-      <OrphaCode>228254</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228254</ExpertLink>
-      <Name lang="nl">Elastoom</Name>
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-      <Name lang="nl">Papula-elastorrhexis</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=228272</ExpertLink>
-      <Name lang="nl">Primaire anetodermie</Name>
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-      <Name lang="nl">Familiale anetodermie</Name>
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-      <OrphaCode>228285</OrphaCode>
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-      <Name lang="nl">Verworven cutis laxa</Name>
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-        <Name lang="nl">Categorie</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="3630">
-      <OrphaCode>2611</OrphaCode>
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-      <Name lang="nl">Lineaire verruceuze naevus-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="19182">
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-          <Name lang="nl">No data available</Name>
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-      <OrphaCode>1309</OrphaCode>
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-      <Name lang="nl">Medullaire sponsnier</Name>
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-      <OrphaCode>231249</OrphaCode>
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-      <Name lang="nl">Hemoglobine E - bèta-thalassemie-syndroom</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23522">
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-      <OrphaCode>231242</OrphaCode>
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-      <OrphaCode>2197</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2197</ExpertLink>
-      <Name lang="nl">Idiopathische hypercalciurie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=231237</ExpertLink>
-      <Name lang="nl">Delta-bèta-thalassemie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=231230</ExpertLink>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=18</ExpertLink>
-      <Name lang="nl">Distale renale tubulaire acidose</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238475</ExpertLink>
-      <Name lang="nl">Familiale hypercholanemie</Name>
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-    <Disorder id="19264">
-      <OrphaCode>238455</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238455</ExpertLink>
-      <Name lang="nl">Infantiele dystonie-parkinsonisme</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19265">
-      <OrphaCode>238459</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238459</ExpertLink>
-      <Name lang="nl">SLC35A1-CDG</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23487">
-          <Name lang="nl">No data available</Name>
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-    <Disorder id="19278">
-      <OrphaCode>238578</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238578</ExpertLink>
-      <Name lang="nl">Familiale klompvoet door 17q23.1q23.2-microduplicatie</Name>
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-        <Name lang="nl">Etiologisch subtype</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="19279">
-      <OrphaCode>238583</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238583</ExpertLink>
-      <Name lang="nl">Hyperfenylalaninemie door deficiëntie van tetrahydrobiopterine</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="19276">
-      <OrphaCode>238557</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238557</ExpertLink>
-      <Name lang="nl">Chuvash-erytrocytose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19277">
-      <OrphaCode>238569</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238569</ExpertLink>
-      <Name lang="nl">Immuundisregulatie - inflammatoire darmziekte - artritis - recidiverende infecties-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19275">
-      <OrphaCode>238547</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238547</ExpertLink>
-      <Name lang="nl">Verworven secundaire polycytemie</Name>
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-        <Name lang="nl">Categorie</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="19272">
-      <OrphaCode>238523</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238523</ExpertLink>
-      <Name lang="nl">Atypisch hypotonie - cystinurie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19273">
-      <OrphaCode>238536</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238536</ExpertLink>
-      <Name lang="nl">Congenitale secundaire polycytemie</Name>
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-        <Name lang="nl">Categorie</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="19287">
-      <OrphaCode>238637</OrphaCode>
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-      <Name lang="nl">Megacystis - mega-ureter-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="19286">
-      <OrphaCode>238624</OrphaCode>
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-      <Name lang="nl">Idiopathische intracraniële hypertensie</Name>
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-    <Disorder id="19285">
-      <OrphaCode>238621</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238621</ExpertLink>
-      <Name lang="nl">Fecale incontinentie gerelateerd aan ileoanale anastomose met pouch</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=238606</ExpertLink>
-      <Name lang="nl">Primaire orthostatische tremor</Name>
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-      <Name lang="nl">IgG4-gerelateerde mesenteritis</Name>
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-      <Name lang="nl">Geïsoleerde deficiëntie van thyrotropinevrijmakend hormoon</Name>
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-      <Name lang="nl">Geïsoleerd congenitaal hypogonadotroop hypogonadisme</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <OrphaCode>240103</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=240103</ExpertLink>
-      <Name lang="nl">Progressieve supranucleaire paralyse - corticobasaal syndroom</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
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-      <OrphaCode>240094</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=240094</ExpertLink>
-      <Name lang="nl">Progressieve supranucleaire paralyse - zuivere akinesie met gangblokkade-syndroom</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="19332">
-      <OrphaCode>240085</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=240085</ExpertLink>
-      <Name lang="nl">Progressieve supranucleaire paralyse - predominant parkinsonisme-syndroom</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
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-      <OrphaCode>240760</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=240760</ExpertLink>
-      <Name lang="nl">Nijmegen-breuksyndroom-achtige aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>331226</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=331226</ExpertLink>
-      <Name lang="nl">Susceptibiliteit voor infectie door TYK2-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23417">
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-      <OrphaCode>331235</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=331235</ExpertLink>
-      <Name lang="nl">Selectieve IgM-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="21992">
-      <OrphaCode>331176</OrphaCode>
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-      <Name lang="nl">Ernstige congenitale neutropenie door G6PC3-deficiëntie</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="21994">
-      <OrphaCode>331187</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=331187</ExpertLink>
-      <Name lang="nl">Immuundeficiëntie door MASP-2-deficiëntie</Name>
-      <DisorderType id="21394">
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="21995">
-      <OrphaCode>331190</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=331190</ExpertLink>
-      <Name lang="nl">Immuundeficiëntie door ficolin3-deficiëntie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
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-          <Name lang="nl">Kindertijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=331206</ExpertLink>
-      <Name lang="nl">Ernstige gecombineerde immuundeficiëntie door volledige RAG1/2-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <Name lang="nl">Chronische actinische dermatitis</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329977</ExpertLink>
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-      <Name lang="nl">Hoogtelongoedeem</Name>
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-      <Name lang="nl">Loodvergiftiging</Name>
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-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-      <Name lang="nl">Hydroa vacciniforme</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21967">
-      <OrphaCode>330061</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=330061</ExpertLink>
-      <Name lang="nl">Actinische prurigo</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21964">
-      <OrphaCode>330050</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=330050</ExpertLink>
-      <Name lang="nl">DNM1L-gerelateerde encefalopathie door defect van mitochondriale en peroxisomale deling</Name>
-      <DisorderType id="21443">
-        <Name lang="nl">Etiologisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21965">
-      <OrphaCode>330054</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=330054</ExpertLink>
-      <Name lang="nl">Congenitaal cataract - progressieve spierhypotonie - gehoorverlies - ontwikkelingsachterstand-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21941">
-      <OrphaCode>329813</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329813</ExpertLink>
-      <Name lang="nl">Mozaïsche genoomwijde paternale uniparentale disomie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21940">
-      <OrphaCode>329802</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329802</ExpertLink>
-      <Name lang="nl">5p13-microduplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21943">
-      <OrphaCode>329883</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329883</ExpertLink>
-      <Name lang="nl">Niet-hypoproteïnemische hypertrofische gastropathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21942">
-      <OrphaCode>329874</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329874</ExpertLink>
-      <Name lang="nl">Idiopathische reuscelmyocarditis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21937">
-      <OrphaCode>329475</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329475</ExpertLink>
-      <Name lang="nl">Spastische paraplegie - botziekte van Paget-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21939">
-      <OrphaCode>329481</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329481</ExpertLink>
-      <Name lang="nl">Lipoproteïne-glomerulopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21938">
-      <OrphaCode>329478</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329478</ExpertLink>
-      <Name lang="nl">Distale myopathie door VCP-mutatie met aanvang op volwassen leeftijd</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21949">
-      <OrphaCode>329942</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329942</ExpertLink>
-      <Name lang="nl">Voorbijgaande neonatale meervoudige acyl-CoA-dehydrogenasedeficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21948">
-      <OrphaCode>329931</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329931</ExpertLink>
-      <Name lang="nl">C3-glomerulonefritis</Name>
-      <DisorderType id="21457">
-        <Name lang="nl">Histopathologisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21951">
-      <OrphaCode>329971</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329971</ExpertLink>
-      <Name lang="nl">Gegeneraliseerde juveniele polyposis/juveniele polyposis coli</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21950">
-      <OrphaCode>329967</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329967</ExpertLink>
-      <Name lang="nl">Intermitterende hydrartrose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21945">
-      <OrphaCode>329894</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329894</ExpertLink>
-      <Name lang="nl">Juveniele overlapmyositis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21947">
-      <OrphaCode>329918</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329918</ExpertLink>
-      <Name lang="nl">C3-glomerulopathie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21946">
-      <OrphaCode>329903</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329903</ExpertLink>
-      <Name lang="nl">Immunoglobuline-gemedieerde membranoproliferatieve glomerulonefritis</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21924">
-      <OrphaCode>329308</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329308</ExpertLink>
-      <Name lang="nl">Neurodegeneratie geassocieerd met vetzuurhydroxylase</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    </Disorder>
-    <Disorder id="21925">
-      <OrphaCode>329314</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329314</ExpertLink>
-      <Name lang="nl">Meervoudig mitochondriaal DNA-deletiesyndroom door DGUOK-deficiëntie met aanvang op volwassen leeftijd</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21926">
-      <OrphaCode>329319</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329319</ExpertLink>
-      <Name lang="nl">Trombocytemie met distale ledemaatdefecten</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21922">
-      <OrphaCode>329284</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329284</ExpertLink>
-      <Name lang="nl">Neurodegeneratie geassocieerd met bèta-propellerproteïne</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
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-    </Disorder>
-    <Disorder id="21933">
-      <OrphaCode>329457</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329457</ExpertLink>
-      <Name lang="nl">Distale artrogrypose type 5D</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="21934">
-      <OrphaCode>329466</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329466</ExpertLink>
-      <Name lang="nl">Autosomaal dominante focale dystonie, DYT25-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <OrphaCode>329469</OrphaCode>
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-      <Name lang="nl">Acute megakaryoblastische leukemie bij kinderen zonder syndroom van Down</Name>
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-      <Name lang="nl">Autosomaal recessieve frontotemporale pachygyrie</Name>
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-      <OrphaCode>329332</OrphaCode>
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-      <OrphaCode>329336</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329336</ExpertLink>
-      <Name lang="nl">Chronische progressieve externe oftalmoplegie met mitochondriale myopathie met aanvang op volwassen leeftijd</Name>
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-          <Name lang="nl">Mitochondriale overerving</Name>
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-      <OrphaCode>329228</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329228</ExpertLink>
-      <Name lang="nl">Microcefale primordiale dwerggroei door ZNF335-deficiëntie</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>329224</OrphaCode>
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-      <Name lang="nl">Syndroom van Schuurs-Hoeijmakers</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329217</ExpertLink>
-      <Name lang="nl">Cerebrale sinoveneuze trombose</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329211</ExpertLink>
-      <Name lang="nl">Autosomaal dominante neovasculaire inflammatoire vitreoretinopathie</Name>
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-      <OrphaCode>329195</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=329195</ExpertLink>
-      <Name lang="nl">Ontwikkelingsachterstand met autismespectrumstoornis en ganginstabiliteit</Name>
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-      <Name lang="nl">Grote gestalte - lange halluces - multipele extra epifysen-syndroom</Name>
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-      <Name lang="nl">Congenitale spierdystrofie met intellectuele achterstand en ernstige epilepsie</Name>
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-      <Name lang="nl">MAGIC-syndroom</Name>
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-      <Name lang="nl">Proteasoom-geassocieerd auto-inflammatoir syndroom</Name>
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-      <OrphaCode>324718</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324718</ExpertLink>
-      <Name lang="nl">ABètaA21G-amyloïdose</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324723</ExpertLink>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324648</ExpertLink>
-      <Name lang="nl">Invasieve niet-tyfoïde salmonellose</Name>
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-      <Name lang="nl">Auto-erytrocyt sensibiliseringssyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="21784">
-      <OrphaCode>324540</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324540</ExpertLink>
-      <Name lang="nl">Afonie - doofheid - retinale dystrofie - gespleten halluces - intellectuele achterstand-syndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="21785">
-      <OrphaCode>324561</OrphaCode>
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-      <Name lang="nl">Hypopigmentatie - puntvormige palmoplantaire keratodermie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="21782">
-      <OrphaCode>324530</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324530</ExpertLink>
-      <Name lang="nl">Auto-inflammatie - PLCG2-geassocieerde antilichaamdeficiëntie - immuundisregulatie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="21783">
-      <OrphaCode>324535</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324535</ExpertLink>
-      <Name lang="nl">Gecombineerde oxidatieve fosforylatiedeficiëntie type 11</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="21781">
-      <OrphaCode>324525</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324525</ExpertLink>
-      <Name lang="nl">Hypertrofische cardiomyopathie met nieranomalieën door mutatie van mitochondriaal DNA</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">No data available</Name>
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-    <Disorder id="21778">
-      <OrphaCode>324442</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324442</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve axonale neuropathie met neuromyotonie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="21776">
-      <OrphaCode>324416</OrphaCode>
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-      <Name lang="nl">Musculaire hypertrofie - hepatomegalie - polyhydramnion-syndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>324422</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324422</ExpertLink>
-      <Name lang="nl">ALG13-CDG</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="21774">
-      <OrphaCode>324410</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324410</ExpertLink>
-      <Name lang="nl">X-gebonden intellectuele achterstand - cardiomegalie - congestief hartfalen-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>324381</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324381</ExpertLink>
-      <Name lang="nl">Erfelijke inclusielichaammyopathie type 4</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-      <OrphaCode>324364</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324364</ExpertLink>
-      <Name lang="nl">Gemengde scleroserende botdystrofie met extra-skeletale manifestaties</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=324353</ExpertLink>
-      <Name lang="nl">Congenitale achiasme</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Sinusknoopdisfunctie en doofheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Ernstige laterale tibiale kromming - kleine gestalte - milde scapula alata - milde faciale dysmorfie-syndroom</Name>
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-      <Name lang="nl">Multipele paragangliomen geassocieerd met polycytemie</Name>
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-      <Name lang="nl">T-cel-immuundeficiëntie met epidermodysplasia verruciformis</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Zuivere of complexe autosomaal dominante spastische paraplegie</Name>
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-        <AverageAgeOfOnset id="23543">
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-      <Name lang="nl">Autosomaal recessieve Mendeliaanse gevoeligheid voor mycobacteriële ziekten door partiële IFNgammaR1-deficiëntie</Name>
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-    <Disorder id="21672">
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-      <Name lang="nl">Mendeliaanse gevoeligheid voor mycobacteriële ziekten door volledige IL12RB1-deficiëntie</Name>
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-      <Name lang="nl">Mendeliaanse gevoeligheid voor mycobacteriële ziekten door volledige IL12B-deficiëntie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="21687">
-      <OrphaCode>319651</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319651</ExpertLink>
-      <Name lang="nl">Constitutionele megaloblastische anemie met ernstige neurologische ziekte</Name>
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-    <Disorder id="21686">
-      <OrphaCode>319646</OrphaCode>
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-      <Name lang="nl">PGM1-CDG</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21685">
-      <OrphaCode>319640</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319640</ExpertLink>
-      <Name lang="nl">Retinale maculadystrofie type 2</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="21684">
-      <OrphaCode>319635</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319635</ExpertLink>
-      <Name lang="nl">Amyloidosis cutis dyschromia</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21681">
-      <OrphaCode>319605</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319605</ExpertLink>
-      <Name lang="nl">X-gebonden Mendeliaanse gevoeligheid voor mycobacteriële ziekten</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="21680">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319600</ExpertLink>
-      <Name lang="nl">Mendeliaanse gevoeligheid voor mycobacteriële ziekten door partiële IRF8-deficiëntie</Name>
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-    <Disorder id="21692">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319678</ExpertLink>
-      <Name lang="nl">Encefalopathie - hypertrofische cardiomyopathie - tubulaire nierziekte-syndroom</Name>
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-      <Name lang="nl">Microcefale primordiale dwerggroei, Dauber-type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21643">
-      <OrphaCode>319308</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319308</ExpertLink>
-      <Name lang="nl">Niercelcarcinoom met translocatie in MiT-familie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21649">
-      <OrphaCode>319332</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319332</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve myogene arthrogryposis multiplex congenita</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21650">
-      <OrphaCode>319340</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319340</ExpertLink>
-      <Name lang="nl">Carney-complex - trismus - pseudocamptodactylie-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21661">
-      <OrphaCode>319487</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319487</ExpertLink>
-      <Name lang="nl">Familiaal papillair of folliculair thyroïdcarcinoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21660">
-      <OrphaCode>319480</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319480</ExpertLink>
-      <Name lang="nl">Acute myeloïde leukemie met somatische CEBPA-mutaties</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="21663">
-      <OrphaCode>319504</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319504</ExpertLink>
-      <Name lang="nl">Gecombineerde oxidatieve fosforylatiedeficiëntie type 8</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21659">
-      <OrphaCode>319465</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319465</ExpertLink>
-      <Name lang="nl">Erfelijke acute myeloïde leukemie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21658">
-      <OrphaCode>319462</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319462</ExpertLink>
-      <Name lang="nl">Hereditair kankerpredispositiesyndroom door biallelische BRCA2-mutaties</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21627">
-      <OrphaCode>319213</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319213</ExpertLink>
-      <Name lang="nl">Lujo hemorragische koorts</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="21624">
-      <OrphaCode>319195</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319195</ExpertLink>
-      <Name lang="nl">Chondro-ectodermale dysplasie met nachtblindheid</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="21625">
-      <OrphaCode>319199</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319199</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve spastische paraplegie type 53</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21630">
-      <OrphaCode>319229</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319229</ExpertLink>
-      <Name lang="nl">Boliviaanse hemorragische koorts</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="21631">
-      <OrphaCode>319234</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319234</ExpertLink>
-      <Name lang="nl">Venezolaanse hemorragische koorts</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="21628">
-      <OrphaCode>319218</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319218</ExpertLink>
-      <Name lang="nl">Ebola hemorragische koorts</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319223</ExpertLink>
-      <Name lang="nl">Argentijnse hemorragische koorts</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="21618">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319160</ExpertLink>
-      <Name lang="nl">Congenitale myopathie met interne nuclei en atypische kernen</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      <OrphaCode>319171</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319171</ExpertLink>
-      <Name lang="nl">Distale 17p13.1-microdeletiesyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319189</ExpertLink>
-      <Name lang="nl">Familiale corticale myoclonus</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
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-      <OrphaCode>319192</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=319192</ExpertLink>
-      <Name lang="nl">Diëncefale-mesencefale junctiedysplasie</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
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-      <Name lang="nl">Syndroom van Wiedemann-Steiner</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="21581">
-      <OrphaCode>317428</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=317428</ExpertLink>
-      <Name lang="nl">Gecombineerde immuundeficiëntie door ORAI1-deficiëntie</Name>
-      <DisorderType id="21450">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="21580">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=317425</ExpertLink>
-      <Name lang="nl">Ernstige gecombineerde immuundeficiëntie door DNA-PKcs-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="21582">
-      <OrphaCode>317430</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=317430</ExpertLink>
-      <Name lang="nl">Gecombineerde immuundeficiëntie door STIM1-deficiëntie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="21585">
-      <OrphaCode>317476</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=317476</ExpertLink>
-      <Name lang="nl">XMEN</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="21549">
-      <OrphaCode>315311</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=315311</ExpertLink>
-      <Name lang="nl">Klassieke congenitale adrenale hyperplasie door deficiëntie van 21-hydroxylase, eenvoudige viriliserende vorm</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21548">
-      <OrphaCode>315306</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=315306</ExpertLink>
-      <Name lang="nl">Klassieke congenitale adrenale hyperplasie door deficiëntie van 21-hydroxylase, vorm met zoutverlies</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="21547">
-      <OrphaCode>314993</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314993</ExpertLink>
-      <Name lang="nl">Cataract - congenitale hartziekte - neuralebuisdefect-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="21546">
-      <OrphaCode>314978</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314978</ExpertLink>
-      <Name lang="nl">X-gebonden niet-progressieve cerebellaire ataxie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="21545">
-      <OrphaCode>314970</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314970</ExpertLink>
-      <Name lang="nl">Lymfoïd hypereosinofiel syndroom</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21544">
-      <OrphaCode>314962</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314962</ExpertLink>
-      <Name lang="nl">Secundair hypereosinofiel syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="21543">
-      <OrphaCode>314950</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314950</ExpertLink>
-      <Name lang="nl">Primair hypereosinofiel syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="21538">
-      <OrphaCode>314918</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314918</ExpertLink>
-      <Name lang="nl">Milde Canavan-Ziekte</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21537">
-      <OrphaCode>314911</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314911</ExpertLink>
-      <Name lang="nl">Ernstige Canavan-ziekte</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21562">
-      <OrphaCode>316235</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=316235</ExpertLink>
-      <Name lang="nl">Autosomaal dominante spastische ataxie</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="21563">
-      <OrphaCode>316240</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=316240</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve spastische ataxie</Name>
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-        <Name lang="nl">Categorie</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21517">
-      <OrphaCode>314701</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314701</ExpertLink>
-      <Name lang="nl">Primaire systemische amyloïdose</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <TypeOfInheritance id="23494">
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-      <OrphaCode>314709</OrphaCode>
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-      <Name lang="nl">Primaire gelokaliseerde amyloïdose</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="21513">
-      <OrphaCode>314679</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314679</ExpertLink>
-      <Name lang="nl">Cerebrofacioarticulair syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
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-      <OrphaCode>314667</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314667</ExpertLink>
-      <Name lang="nl">TMEM165-CDG</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>314689</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314689</ExpertLink>
-      <Name lang="nl">Gecombineerde immuundeficiëntie door STK4-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
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-      <TypeOfInheritanceList count="1">
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="21509">
-      <OrphaCode>314652</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314652</ExpertLink>
-      <Name lang="nl">Variant ABèta2M-amyloïdose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
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-    <Disorder id="21508">
-      <OrphaCode>314647</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314647</ExpertLink>
-      <Name lang="nl">Niet-progressieve cerebellaire ataxie met intellectuele achterstand</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
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-        <AverageAgeOfOnset id="23522">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="21511">
-      <OrphaCode>314662</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314662</ExpertLink>
-      <Name lang="nl">Segmentaal progressief overgroeisyndroom met fibroadipose hyperplasie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314655</ExpertLink>
-      <Name lang="nl">Ernstige neonatale hypotonie - insulten - encefalopathie-syndroom door 5q31.3-microdeletie</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
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-      <OrphaCode>314621</OrphaCode>
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-      <Name lang="nl">Duplicatie van hypofyse</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>370034</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370034</ExpertLink>
-      <Name lang="nl">Familiale syringomyelie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22469">
-      <OrphaCode>370039</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370039</ExpertLink>
-      <Name lang="nl">Angorahaarnaevus</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22466">
-      <OrphaCode>370022</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370022</ExpertLink>
-      <Name lang="nl">Ataxie - intellectuele achterstand - oculomotorische apraxie - cerebellaire cysten-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22467">
-      <OrphaCode>370026</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370026</ExpertLink>
-      <Name lang="nl">Acute myeloïde leukemie met t(8;16)(p11;p13) translocatie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22464">
-      <OrphaCode>370015</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370015</ExpertLink>
-      <Name lang="nl">Spondylo-epimetafysaire dysplasie, Isidor-Toutain-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22479">
-      <OrphaCode>370088</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370088</ExpertLink>
-      <Name lang="nl">Acuut infantiel leverfalen - multisystemische betrokkenheid-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22476">
-      <OrphaCode>370076</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370076</ExpertLink>
-      <Name lang="nl">Foetaal carbamazepinesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22477">
-      <OrphaCode>370079</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370079</ExpertLink>
-      <Name lang="nl">Proximale 16p11.2-microduplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22472">
-      <OrphaCode>370052</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370052</ExpertLink>
-      <Name lang="nl">SCALP-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22513">
-      <OrphaCode>371007</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=371007</ExpertLink>
-      <Name lang="nl">Congenitale spierdystrofie met hyperlaxiteit</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22512">
-      <OrphaCode>370997</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370997</ExpertLink>
-      <Name lang="nl">Spier-oog-hersenziekte met bilaterale multicystische leukodystrofie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22500">
-      <OrphaCode>370921</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370921</ExpertLink>
-      <Name lang="nl">STT3A-CDG</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22501">
-      <OrphaCode>370924</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370924</ExpertLink>
-      <Name lang="nl">STT3B-CDG</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22502">
-      <OrphaCode>370927</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370927</ExpertLink>
-      <Name lang="nl">SSR4-CDG</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22503">
-      <OrphaCode>370930</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370930</ExpertLink>
-      <Name lang="nl">XYLT1-CDG</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22509">
-      <OrphaCode>370959</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370959</ExpertLink>
-      <Name lang="nl">Congenitale spierdystrofie met cerebellaire betrokkenheid</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22510">
-      <OrphaCode>370968</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370968</ExpertLink>
-      <Name lang="nl">Congenitale spierdystrofie met intellectuele achterstand</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22511">
-      <OrphaCode>370980</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370980</ExpertLink>
-      <Name lang="nl">Congenitale musculaire dystrofie zonder intellectuele achterstand</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22504">
-      <OrphaCode>370933</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370933</ExpertLink>
-      <Name lang="nl">GM3-synthasedeficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22507">
-      <OrphaCode>370943</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=370943</ExpertLink>
-      <Name lang="nl">Autismespectrumstoornis - epilepsie - artrogrypose-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22449">
-      <OrphaCode>369929</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=369929</ExpertLink>
-      <Name lang="nl">Primair hyperaldosteronisme - insulten - neurologische anomalieën-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23494">
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-      <OrphaCode>369920</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=369920</ExpertLink>
-      <Name lang="nl">Pontocerebellaire hypoplasie type 9</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22451">
-      <OrphaCode>369942</OrphaCode>
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-      <Name lang="nl">CADDS</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Ernstige motorische en intellectuele achterstand - sensorineurale doofheid - dystonie-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22453">
-      <OrphaCode>369955</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=369955</ExpertLink>
-      <Name lang="nl">Methylmalonacidurie met homocystinurie, type cblJ</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>369950</OrphaCode>
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-      <Name lang="nl">Intellectuele achterstand - insulten - macrocefalie - obesitas-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-      <OrphaCode>369970</OrphaCode>
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-      <Name lang="nl">Microcornea - myopische chorioretinale atrofie - telecanthus-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>369962</OrphaCode>
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-      <Name lang="nl">Methylmalonacidurie met homocystinurie, type cblX</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-      <OrphaCode>369979</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=369979</ExpertLink>
-      <Name lang="nl">Hyperfalangie van vingers - teenanomalieën - ernstige pectus excavatum-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Ernstige dermatitis - meervoudige allergieën - metabole aftakeling-syndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <Name lang="nl">Focale palmoplantaire keratodermie met keratosen van gewrichten</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Diffuse palmoplantaire keratodermie met pijnlijke fissuren</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Intellectuele achterstand - faciale dysmorfie - handanomalieën-syndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Intellectuele achterstand - insulten - hypofosfatasie - oftalmische-skeletale anomalieën-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">TRAPPC11-gerelateerde limb-girdle-spierdystrofie R18</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Congenitale sideroblastische anemie - B-cel-immuundeficiëntie - periodieke koorts - ontwikkelingsachterstand-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Autosomaal recessieve intermediaire ziekte van Charcot-Marie-Tooth type C</Name>
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-      <Name lang="nl">Primaire niet-essentiële cutis verticis gyrata</Name>
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-      <Name lang="nl">Gecombineerde immuundeficiëntie door CARD11-deficiëntie</Name>
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-      <OrphaCode>357502</OrphaCode>
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-      <Name lang="nl">Idiopathisch nefrotisch syndroom</Name>
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-      <Name lang="nl">D,L-2-hydroxyglutaaracidurie</Name>
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-      <Name lang="nl">SLC35A2-CDG</Name>
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-      <Name lang="nl">Hemolytisch-uremisch syndroom met DGKE-deficiëntie</Name>
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-      <Name lang="nl">19p13.13-microdeletiesyndroom</Name>
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-      <OrphaCode>356996</OrphaCode>
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-      <Name lang="nl">ANK3-gerelateerd intellectuele achterstand - slaapstoornis-syndroom</Name>
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-      <Name lang="nl">Letale occipitale encefalocele - skeletdysplasie-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=293202</ExpertLink>
-      <Name lang="nl">Epithelioïd sarcoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="20847">
-      <OrphaCode>293284</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=293284</ExpertLink>
-      <Name lang="nl">Tetrahydrobiopterineresponsieve hyperfenylalaninemie/fenylketonurie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="20846">
-      <OrphaCode>293208</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=293208</ExpertLink>
-      <Name lang="nl">Compressie van truncus coeliacus-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="5522">
-      <OrphaCode>2459</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2459</ExpertLink>
-      <Name lang="nl">Mansonelliasis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="5521">
-      <OrphaCode>2404</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2404</ExpertLink>
-      <Name lang="nl">Loiasis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="5520">
-      <OrphaCode>2394</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2394</ExpertLink>
-      <Name lang="nl">Pyruvaatdehydrogenase E3-deficiëntie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="5527">
-      <OrphaCode>2356</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2356</ExpertLink>
-      <Name lang="nl">Arachnoïdale cyste</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="5525">
-      <OrphaCode>829</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=829</ExpertLink>
-      <Name lang="nl">Ziekte van Still met aanvang op volwassen leeftijd</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="5530">
-      <OrphaCode>3096</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3096</ExpertLink>
-      <Name lang="nl">Syndroom van Reye</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="5529">
-      <OrphaCode>1929</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1929</ExpertLink>
-      <Name lang="nl">Subacute encefalitis van Rasmussen</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="5528">
-      <OrphaCode>1183</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=1183</ExpertLink>
-      <Name lang="nl">Opsoclonus - myoclonus-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="5535">
-      <OrphaCode>2688</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2688</ExpertLink>
-      <Name lang="nl">Volwassen idiopathische neutropenie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="5534">
-      <OrphaCode>2686</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2686</ExpertLink>
-      <Name lang="nl">Cyclische neutropenie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="5533">
-      <OrphaCode>890</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=890</ExpertLink>
-      <Name lang="nl">Veno-occlusieve ziekte van lever</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="5532">
-      <OrphaCode>176</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=176</ExpertLink>
-      <Name lang="nl">Niet-rhizomele chondrodysplasia punctata</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
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-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23445">
-          <Name lang="nl">X-gebonden dominant</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="5518">
-      <OrphaCode>231</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=231</ExpertLink>
-      <Name lang="nl">Dracunculiasis</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="5519">
-      <OrphaCode>2035</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2035</ExpertLink>
-      <Name lang="nl">Lymfatische filariasis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=284448</ExpertLink>
-      <Name lang="nl">CLIPPERS</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <OrphaCode>284454</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=284454</ExpertLink>
-      <Name lang="nl">Acute zonale occulte perifere retinopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        </TypeOfInheritance>
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-    <Disorder id="20614">
-      <OrphaCode>284460</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=284460</ExpertLink>
-      <Name lang="nl">Acute ringvormige perifere retinopathie</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="20608">
-      <OrphaCode>284414</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=284414</ExpertLink>
-      <Name lang="nl">Glycerolkinasedeficiëntie, volwassen vorm</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=284417</ExpertLink>
-      <Name lang="nl">Deficiëntie van fosfoserine-aminotransferase, infantiele/juveniele vorm</Name>
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-        <AverageAgeOfOnset id="23522">
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>284426</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=284426</ExpertLink>
-      <Name lang="nl">Glycogeenstapelingsziekte door deficiëntie van lactaatdehydrogenase M-subeenheid</Name>
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-      <Name lang="nl">Idiopathische panuveïtis</Name>
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-      <Name lang="nl">Occipitale pachygyrie en polymicrogyrie</Name>
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-      <Name lang="nl">Autosomaal recessieve nageldysplasie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280779</ExpertLink>
-      <Name lang="nl">Cutane collageneuze vasculopathie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280785</ExpertLink>
-      <Name lang="nl">Bulleuze diffuse cutane mastocytose</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280794</ExpertLink>
-      <Name lang="nl">Pseudoxanthomateuze diffuse cutane mastocytose</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="20497">
-      <OrphaCode>280679</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280679</ExpertLink>
-      <Name lang="nl">Moyamoya-angiopathie - kleine gestalte - faciale dysmorfie - hypergonadotroop hypogonadisme-syndroom</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">X-gebonden recessief</Name>
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-      <OrphaCode>280763</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280763</ExpertLink>
-      <Name lang="nl">Ernstige intellectuele achterstand en progressieve spastische paraplegie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>280774</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280774</ExpertLink>
-      <Name lang="nl">Gegeneraliseerde essentiële teleangiëctasie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280840</ExpertLink>
-      <Name lang="nl">Congenitale malformatie van pulmonale luchtwegen type 2</Name>
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-      <OrphaCode>280847</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280847</ExpertLink>
-      <Name lang="nl">Congenitale malformatie van pulmonale luchtwegen type 3</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=280854</ExpertLink>
-      <Name lang="nl">Congenitale malformatie van pulmonale luchtwegen type 4</Name>
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-      <Name lang="nl">IgG4-gerelateerde ziekte</Name>
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-      <Name lang="nl">Interstitiële tumor van foetale long</Name>
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-      <Name lang="nl">Glycerolkinasedeficiëntie, juveniele vorm</Name>
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-      <Name lang="nl">FGFR2-gerelateerde gebogen botdysplasie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=313846</ExpertLink>
-      <Name lang="nl">Familiale cutane teleangiëctasie en orofaryngeale kankerpredispositiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=313800</ExpertLink>
-      <Name lang="nl">Retinadystrofie - oedeem van nervus opticus - splenomegalie - anhidrose - migrainehoofdpijn-syndroom</Name>
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-      <Name lang="nl">Erfelijke diffuse leuko-encefalopathie met axonale sferoïden en gepigmenteerde glia</Name>
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-      <OrphaCode>314555</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314555</ExpertLink>
-      <Name lang="nl">Faciale dysmorfie - oculaire anomalieën - osteopenie - intellectuele achterstand - dentale anomalieën-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21489">
-      <OrphaCode>314466</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314466</ExpertLink>
-      <Name lang="nl">Atypisch syndroom van Meigs</Name>
-      <DisorderType id="21422">
-        <Name lang="nl">Klinisch syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21488">
-      <OrphaCode>314459</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314459</ExpertLink>
-      <Name lang="nl">Pseudo-Meigssyndroom</Name>
-      <DisorderType id="21422">
-        <Name lang="nl">Klinisch syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21491">
-      <OrphaCode>314478</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314478</ExpertLink>
-      <Name lang="nl">Ovarieel fibrothecoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21490">
-      <OrphaCode>314473</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314473</ExpertLink>
-      <Name lang="nl">Ovarieel fibroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21484">
-      <OrphaCode>314422</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314422</ExpertLink>
-      <Name lang="nl">Ameloblastisch carcinoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21486">
-      <OrphaCode>314432</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314432</ExpertLink>
-      <Name lang="nl">Hernia spiegeli - cryptorchidie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21487">
-      <OrphaCode>314451</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314451</ExpertLink>
-      <Name lang="nl">Syndroom van Meigs</Name>
-      <DisorderType id="21422">
-        <Name lang="nl">Klinisch syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21480">
-      <OrphaCode>314394</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314394</ExpertLink>
-      <Name lang="nl">Kleine gestalte - onychodysplasie - faciale dysmorfie - hypotrichose-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21481">
-      <OrphaCode>314399</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314399</ExpertLink>
-      <Name lang="nl">Autosomaal dominante aplasie en myelodysplasie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21482">
-      <OrphaCode>314404</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314404</ExpertLink>
-      <Name lang="nl">Autosomaal dominante cerebellaire ataxie - doofheid - narcolepsie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21483">
-      <OrphaCode>314419</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314419</ExpertLink>
-      <Name lang="nl">Ameloblastoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21476">
-      <OrphaCode>314373</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314373</ExpertLink>
-      <Name lang="nl">Chronische infantiele diarree door guanylaatcyclase 2C-overactiviteit</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21477">
-      <OrphaCode>314376</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314376</ExpertLink>
-      <Name lang="nl">Intestinale obstructie bij neonaat door gyanylaatcyclase 2C-deficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21478">
-      <OrphaCode>314381</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314381</ExpertLink>
-      <Name lang="nl">Erfelijke sensorische en autonome neuropathie type 6</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21479">
-      <OrphaCode>314389</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314389</ExpertLink>
-      <Name lang="nl">Xq12-q13.3-duplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21472">
-      <OrphaCode>314034</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314034</ExpertLink>
-      <Name lang="nl">7p22.1-microduplicatiesyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21474">
-      <OrphaCode>314041</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314041</ExpertLink>
-      <Name lang="nl">Marfanoïde habitus - liesbreuk - gevorderde botleeftijd-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21475">
-      <OrphaCode>314051</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=314051</ExpertLink>
-      <Name lang="nl">Leuko-encefalopathie - anomalieën van thalamus en hersenstam - hoog lactaatgehalte-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23487">
-          <Name lang="nl">No data available</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21251">
-      <OrphaCode>306682</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306682</ExpertLink>
-      <Name lang="nl">Mangaanvergiftiging</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21249">
-      <OrphaCode>306674</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306674</ExpertLink>
-      <Name lang="nl">Syndroom van Kufor-Rakeb</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21248">
-      <OrphaCode>306669</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306669</ExpertLink>
-      <Name lang="nl">Hemiparkinsonisme-hemiatrofie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21253">
-      <OrphaCode>306692</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306692</ExpertLink>
-      <Name lang="nl">Parkinsonisme-dystonie geïnduceerd door cyanide</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21252">
-      <OrphaCode>306686</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306686</ExpertLink>
-      <Name lang="nl">Vertraagde encefalopathie door intoxicatie door koolmonoxide</Name>
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-      <Name lang="nl">Hemidystonie-hemiatrofie-syndroom</Name>
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-      <Name lang="nl">Primaire dystonie, DYT21-type</Name>
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-    <Disorder id="21260">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306731</ExpertLink>
-      <Name lang="nl">Sydenhamchorea</Name>
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-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="21301">
-      <OrphaCode>308166</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308166</ExpertLink>
-      <Name lang="nl">Erythrokeratodermie variabilis progressiva</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="21305">
-      <OrphaCode>308380</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308380</ExpertLink>
-      <Name lang="nl">Methylcobalaminedeficiëntie type cblDv1</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21306">
-      <OrphaCode>308386</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308386</ExpertLink>
-      <Name lang="nl">Sulfietoxidasedeficiëntie door molybdeen-cofactordeficiëntie type A</Name>
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-        <Name lang="nl">Etiologisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21307">
-      <OrphaCode>308393</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308393</ExpertLink>
-      <Name lang="nl">Sulfietoxidasedeficiëntie door molybdeen-cofactordeficiëntie type B</Name>
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-        <Name lang="nl">Etiologisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21308">
-      <OrphaCode>308400</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308400</ExpertLink>
-      <Name lang="nl">Sulfietoxidasedeficiëntie door molybdeen-cofactordeficiëntie type C</Name>
-      <DisorderType id="21443">
-        <Name lang="nl">Etiologisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21310">
-      <OrphaCode>308410</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308410</ExpertLink>
-      <Name lang="nl">Autisme - epilepsie-syndroom door deficiëntie van vertakte keten-ketozuurdehydrogenasekinase</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21311">
-      <OrphaCode>308425</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308425</ExpertLink>
-      <Name lang="nl">Methylmalonacidurie door methylmalonyl-CoA-epimerasedeficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21283">
-      <OrphaCode>307766</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=307766</ExpertLink>
-      <Name lang="nl">Gekruld haar-acrale keratodermie-cariës-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="21285">
-      <OrphaCode>307804</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=307804</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve ziekte met diffuse palmoplantaire keratodermie als hoofdkenmerk</Name>
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-        <Name lang="nl">Categorie</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>307773</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=307773</ExpertLink>
-      <Name lang="nl">Autosomaal dominante diffuse mutilerende palmoplantaire keratodermie</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <Name lang="nl">Hypotrichose-osteolyse-periodontitis-palmoplantaire keratodermie-syndroom</Name>
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-      <Name lang="nl">Marginale papuleuze palmoplantaire keratodermie</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-      <Name lang="nl">Autosomaal recessieve ziekte geassocieerd met puntvormige palmoplantaire keratodermie als hoofdkenmerk</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308031</ExpertLink>
-      <Name lang="nl">Autosomaal dominante ziekte geassocieerd met puntvormige palmoplantaire keratodermie als hoofdkenmerk</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <TypeOfInheritance id="23410">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308698</ExpertLink>
-      <Name lang="nl">Glycogeenstapelingsziekte type 4, neuromusculaire vorm op kinderleeftijd</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <Name lang="nl">Glycogeenstapelingsziekte type 4, volwassen neuromusculaire vorm</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308684</ExpertLink>
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-        <AverageAgeOfOnset id="23515">
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-      <Name lang="nl">Deficiëntie van mevalonaatkinase</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=309015</ExpertLink>
-      <Name lang="nl">Familiale deficiëntie van lipoproteïnelipase</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21337">
-      <OrphaCode>309020</OrphaCode>
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-      <Name lang="nl">Familiale deficiëntie van apolipoproteïne C-II</Name>
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-        <Name lang="nl">Etiologisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>308487</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308487</ExpertLink>
-      <Name lang="nl">Gegeneraliseerde galactose-epimerasedeficiëntie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <OrphaCode>178</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=178</ExpertLink>
-      <Name lang="nl">Chordoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308473</ExpertLink>
-      <Name lang="nl">Erytrocyt galactose-epimerasedeficiëntie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=2637</ExpertLink>
-      <Name lang="nl">Microcefale osteodysplastische primordiale dwerggroei type II</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>592</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=592</ExpertLink>
-      <Name lang="nl">Macrofagische myofasciitis</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308442</ExpertLink>
-      <Name lang="nl">Vitamine B12-responsieve methylmalonacidemie, type cblDv2</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <OrphaCode>308655</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308655</ExpertLink>
-      <Name lang="nl">Glycogeenstapelingsziekte type 4, fatale perinatale neuromusculaire vorm</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308638</ExpertLink>
-      <Name lang="nl">Glycogeenstapelingsziekte type 4, niet-progressieve hepatische vorm</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=308621</ExpertLink>
-      <Name lang="nl">Glycogeenstapelingsziekte type 4, progressieve hepatische vorm</Name>
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-      <Name lang="nl">Glycogeenstapelingsziekte door zure-maltasedeficiëntie, infantiele aanvang</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306658</ExpertLink>
-      <Name lang="nl">Familiale normofosfatemische tumorale calcinose</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21243">
-      <OrphaCode>306644</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306644</ExpertLink>
-      <Name lang="nl">Complicatie na orgaantransplantatie</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="21239">
-      <OrphaCode>306617</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306617</ExpertLink>
-      <Name lang="nl">X-gebonden gecompliceerde spastische paraplegie type 1</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21236">
-      <OrphaCode>306577</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306577</ExpertLink>
-      <Name lang="nl">Hereditaire natriumkanalopathie-gerelateerde dunnevezelneuropathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21232">
-      <OrphaCode>306558</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=306558</ExpertLink>
-      <Name lang="nl">Primaire microcefalie - epilepsie - permanente neonatale diabetes-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21043">
-      <OrphaCode>295195</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=295195</ExpertLink>
-      <Name lang="nl">Synpolydactylie type 1</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="21041">
-      <OrphaCode>295191</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=295191</ExpertLink>
-      <Name lang="nl">Zygodactylie type 3</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21046">
-      <OrphaCode>295201</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=295201</ExpertLink>
-      <Name lang="nl">Congenitale verticale talus, unilateraal</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21047">
-      <OrphaCode>295203</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=295203</ExpertLink>
-      <Name lang="nl">Congenitale verticale talus, bilateraal</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="21044">
-      <OrphaCode>295197</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=295197</ExpertLink>
-      <Name lang="nl">Synpolydactylie type 2</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="21064">
-      <OrphaCode>295239</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=295239</ExpertLink>
-      <Name lang="nl">Macrodactylie van vinger, unilateraal</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="21066">
-      <OrphaCode>295243</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=295243</ExpertLink>
-      <Name lang="nl">Macrodactylie van tenen, unilateraal</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
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-    <Disorder id="21080">
-      <OrphaCode>298644</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=298644</ExpertLink>
-      <Name lang="nl">Stoornis van thiaminemetabolisme en -transport</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="21100">
-      <OrphaCode>300179</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=300179</ExpertLink>
-      <Name lang="nl">Kyfoscoliotisch syndroom van Ehlers-Danlos door FKBP22-deficiëntie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=300319</ExpertLink>
-      <Name lang="nl">Ziekte van Charcot-Marie-Tooth type 2P</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-          <Name lang="nl">Puber</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=300324</ExpertLink>
-      <Name lang="nl">Persisterende polyklonale B-cellymfocytose</Name>
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-          <Name lang="nl">No data available</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=300313</ExpertLink>
-      <Name lang="nl">Congenitaal cataract - gehoorverlies - ernstige ontwikkelingsachterstand-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=300298</ExpertLink>
-      <Name lang="nl">Ernstige congenitale hypochrome anemie met ringsideroblasten</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Aandoening van bindweefsel door lysylhydroxylase 3-deficiëntie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=300293</ExpertLink>
-      <Name lang="nl">Transiënte infantiele hypertriglyceridemie en hepatosteatose</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=300385</ExpertLink>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-      <OrphaCode>464370</OrphaCode>
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-      <Name lang="nl">Intoxicatie door paracetamol</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=662</ExpertLink>
-      <Name lang="nl">Lymfoedeem met gele nagels</Name>
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-      <OrphaCode>537</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=537</ExpertLink>
-      <Name lang="nl">Toxische epidermale necrolyse</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <Name lang="nl">SAPHO-syndroom</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-      <OrphaCode>456298</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=456298</ExpertLink>
-      <Name lang="nl">1p35.2-microdeletiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">X-gebonden myotubulaire myopathie - abnormale genitaliën-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Infantiele multisystemische neurologische-endocriene-pancreatische ziekte</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <Name lang="nl">Erfelijke sensorische neuropathie - doofheid - dementie-syndroom</Name>
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-      <Name lang="nl">NTHL1-gerelateerde geattenueerde familiale adenomateuze polyposis</Name>
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-      <Name lang="nl">Acuut stralingssyndroom</Name>
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-      <OrphaCode>454706</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=454706</ExpertLink>
-      <Name lang="nl">Progressieve spieratrofie</Name>
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-      <Name lang="nl">Verworven ziekte van Creutzfeldt-Jakob</Name>
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-      <Name lang="nl">Primaire cutane plasmocytose</Name>
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-      <Name lang="nl">Cutaan pseudolymfoom</Name>
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-      <Name lang="nl">Familiale congenitale obstructie van ductus nasolacrimalis</Name>
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-      <OrphaCode>453499</OrphaCode>
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-      <OrphaCode>453510</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=453510</ExpertLink>
-      <Name lang="nl">Congenitale ongevoeligheid voor pijn met ernstige intellectuele achterstand</Name>
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-      <Name lang="nl">Scedosporiose</Name>
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-      <Name lang="nl">Ziekte door zikavirus</Name>
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-      <Name lang="nl">Progressieve scapulohumerale peroneale distale myopathie</Name>
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-      <Name lang="nl">Spinocerebellaire ataxie type 41</Name>
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-    <Disorder id="23733">
-      <OrphaCode>457485</OrphaCode>
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-      <Name lang="nl">Macrocefalie - intellectuele achterstand - neurologische ontwikkelingsstoornis - kleine thorax-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457265</ExpertLink>
-      <Name lang="nl">Progressieve myoclonische epilepsie type 9</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="23719">
-      <OrphaCode>457279</OrphaCode>
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-      <Name lang="nl">Intellectuele achterstand - macrocefalie - hypotonie - gedragsstoornissen-syndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>457260</OrphaCode>
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-      <Name lang="nl">X-gebonden intellectuele achterstand - hypotonie - bewegingsstoornis-syndroom</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="23714">
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-      <Name lang="nl">X-gebonden intellectuele achterstand - kleine gestalte - overgewicht-syndroom</Name>
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457246</ExpertLink>
-      <Name lang="nl">Heldercellig sarcoom van nier</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23522">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457395</ExpertLink>
-      <Name lang="nl">Progressieve spondylo-epimetafysaire dyplasie - kleine gestalte - korte vierde metatarsalen - intellectuele achterstand-syndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23727">
-      <OrphaCode>457406</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457406</ExpertLink>
-      <Name lang="nl">Multipele mitochondriale disfuncties-syndroom type 4</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23724">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457375</ExpertLink>
-      <Name lang="nl">ITPA-gerelateerde letale infantiele neurologische stoornis met cataract en cardiale betrokkenheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457378</ExpertLink>
-      <Name lang="nl">Complexe letale osteochondrodysplasie</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <Name lang="nl">Megalencefalie - ernstige kyfoscoliose - overgroei-syndroom</Name>
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-        <AverageAgeOfOnset id="23515">
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-      <TypeOfInheritanceList count="1">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=457365</ExpertLink>
-      <Name lang="nl">Intellectuele achterstand - spierzwakte - kleine gestalte - faciale dysmorfie-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Geïsoleerde splenogonadale fusie</Name>
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-      <OrphaCode>457223</OrphaCode>
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-      <Name lang="nl">Geïsoleerde gegeneraliseerde anhidrose met normale zweetklieren</Name>
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-    <Disorder id="22939">
-      <OrphaCode>404560</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404560</ExpertLink>
-      <Name lang="nl">Familiaal melanoom met atypische meervoudige moedervlekken-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
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-    <Disorder id="22938">
-      <OrphaCode>404553</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404553</ExpertLink>
-      <Name lang="nl">Deficiëntie van adenosinedeaminase 2</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22937">
-      <OrphaCode>404546</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404546</ExpertLink>
-      <Name lang="nl">DITRA</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22935">
-      <OrphaCode>404521</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404521</ExpertLink>
-      <Name lang="nl">Spinale spieratrofie met ademhalingsnood type 2</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="22934">
-      <OrphaCode>404514</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404514</ExpertLink>
-      <Name lang="nl">Niercelcarcinoom geassocieerd met verworven cystische ziekte</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="22932">
-      <OrphaCode>404507</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404507</ExpertLink>
-      <Name lang="nl">Chondromyxoïd fibroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="22931">
-      <OrphaCode>404499</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404499</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve cerebellaire ataxie - epilepsie - intellectuele achterstand-syndroom door RUBCN-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22930">
-      <OrphaCode>404493</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404493</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve cerebellaire ataxie - epilepsie - intellectuele achterstand-syndroom door TUD-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22929">
-      <OrphaCode>404481</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404481</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve cerebellaire ataxie - epilepsie - intellectuele achterstand-syndroom</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="22928">
-      <OrphaCode>404476</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=404476</ExpertLink>
-      <Name lang="nl">Algehele ontwikkelingsachterstand - longcysten - overgroei - Wilmstumor-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
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-    <Disorder id="23016">
-      <OrphaCode>411527</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411527</ExpertLink>
-      <Name lang="nl">Veneuze stamocclusie van retina</Name>
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-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="23018">
-      <OrphaCode>411536</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411536</ExpertLink>
-      <Name lang="nl">Milde fosforibosylpyrofosfaat-synthetase-superactiviteit</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-      <OrphaCode>411543</OrphaCode>
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-      <Name lang="nl">Ernstige fosforibosylpyrofosfaat-synthetase-superactiviteit</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-    <Disorder id="23020">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411590</ExpertLink>
-      <Name lang="nl">Wolfram-achtig syndroom</Name>
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-      <OrphaCode>411593</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411593</ExpertLink>
-      <Name lang="nl">Insuline-auto-immuun syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
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-          <Name lang="nl">Volwassenheid</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411602</ExpertLink>
-      <Name lang="nl">Erfelijke ziekte van Parkinson met late aanvang</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="23023">
-      <OrphaCode>411629</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411629</ExpertLink>
-      <Name lang="nl">Infantiele nefropathische cystinose</Name>
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-    <Disorder id="23012">
-      <OrphaCode>411493</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411493</ExpertLink>
-      <Name lang="nl">Pontocerebellaire hypoplasie type 10</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">Syndroom van Williams-Campbell</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=411511</ExpertLink>
-      <Name lang="nl">Syndroom van Angelman door puntmutatie</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-      <Name lang="nl">Syndroom van Angelman door imprintingsdefect in 15q11-q13</Name>
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-      <Name lang="nl">Distale myopathie met aanvang in bovenste ledematen, Fins type</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22746">
-      <OrphaCode>399081</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=399081</ExpertLink>
-      <Name lang="nl">KLHL9-gerelateerde distale myopathie met aanvang tijdens de kindertijd</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="22749">
-      <OrphaCode>399103</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=399103</ExpertLink>
-      <Name lang="nl">Distale nebulinemyopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22748">
-      <OrphaCode>399096</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=399096</ExpertLink>
-      <Name lang="nl">Distale anoctaminopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="22739">
-      <OrphaCode>398934</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398934</ExpertLink>
-      <Name lang="nl">Maligne epitheliale tumor van ovarium</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22741">
-      <OrphaCode>398961</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398961</ExpertLink>
-      <Name lang="nl">Mucineus adenocarcinoom van ovarium</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22740">
-      <OrphaCode>398940</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398940</ExpertLink>
-      <Name lang="nl">Maligne niet-epitheliale tumor van ovarium</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22742">
-      <OrphaCode>398971</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398971</ExpertLink>
-      <Name lang="nl">Heldercellig adenocarcinoom van ovarium</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22728">
-      <OrphaCode>398124</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398124</ExpertLink>
-      <Name lang="nl">Neonatale lupus erythematosus</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22729">
-      <OrphaCode>398127</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398127</ExpertLink>
-      <Name lang="nl">Neonatale sclerodermie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22730">
-      <OrphaCode>398147</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398147</ExpertLink>
-      <Name lang="nl">Persisterende idiopathische aangezichtspijn</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22731">
-      <OrphaCode>398156</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398156</ExpertLink>
-      <Name lang="nl">Oculo-auriculo-fronto-nasaal syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22732">
-      <OrphaCode>398166</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398166</ExpertLink>
-      <Name lang="nl">Focale faciale dermale dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="22733">
-      <OrphaCode>398173</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398173</ExpertLink>
-      <Name lang="nl">Focale faciale dermale dysplasie type II</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22734">
-      <OrphaCode>398189</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398189</ExpertLink>
-      <Name lang="nl">Focale faciale dermale dysplasie type IV</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    </Disorder>
-    <Disorder id="22720">
-      <OrphaCode>398069</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398069</ExpertLink>
-      <Name lang="nl">Syndroom van Schaaf-Yang</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22721">
-      <OrphaCode>398073</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398073</ExpertLink>
-      <Name lang="nl">Prader-Willi-achtig syndroom</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="22722">
-      <OrphaCode>398079</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398079</ExpertLink>
-      <Name lang="nl">SIM1-gerelateerd Prader-Willi-achtig syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="22723">
-      <OrphaCode>398088</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398088</ExpertLink>
-      <Name lang="nl">Hereditaire cryohydrocytose met normaal stomatine</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="22724">
-      <OrphaCode>398091</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398091</ExpertLink>
-      <Name lang="nl">Secundaire neonatale auto-immune ziekte</Name>
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-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
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-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="22725">
-      <OrphaCode>398097</OrphaCode>
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-      <Name lang="nl">Neonataal antifosfolipidensyndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="22726">
-      <OrphaCode>398109</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398109</ExpertLink>
-      <Name lang="nl">Neonatale auto-immune hemolytische anemie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="22727">
-      <OrphaCode>398117</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=398117</ExpertLink>
-      <Name lang="nl">Neonatale dermatomyositis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="23306">
-      <OrphaCode>435628</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=435628</ExpertLink>
-      <Name lang="nl">Syndroom van Keppen-Lubinsky</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="23311">
-      <OrphaCode>435743</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=435743</ExpertLink>
-      <Name lang="nl">Congenitale urachale anomalie</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
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-      <Name lang="nl">Pseudoxanthoma elasticum-achtige huidmanifestaties met retinitis pigmentosa</Name>
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-      <Name lang="nl">Autosomaal recessieve primaire immuundeficiëntie met defecte spontane natuurlijke killercel-cytotoxiciteit</Name>
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-      <Name lang="nl">Deficiëntie van vetzuur-acyl-CoA-reductase 1</Name>
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-      <Name lang="nl">PCNA-gerelateerde progressieve neurodegeneratieve fotosensitiviteit-syndroom</Name>
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-      <Name lang="nl">Syndroom van Steel</Name>
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-      <Name lang="nl">Ketoacidose als gevolg van monocarboxylaattransporter 1-deficiëntie</Name>
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-    <Disorder id="23376">
-      <OrphaCode>439167</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439167</ExpertLink>
-      <Name lang="nl">Placentale insufficiëntie</Name>
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-        <Name lang="nl">Klinisch syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439175</ExpertLink>
-      <Name lang="nl">Pediatrische arteriële ischemische beroerte</Name>
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-        <Name lang="nl">Klinisch syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="23390">
-      <OrphaCode>439762</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439762</ExpertLink>
-      <Name lang="nl">Systemische polyarteriitis nodosa</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <OrphaCode>439822</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439822</ExpertLink>
-      <Name lang="nl">Syndroom door PDE4D-haploinsufficiëntie</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="23388">
-      <OrphaCode>439746</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439746</ExpertLink>
-      <Name lang="nl">Secundaire polyarteriitis nodosa</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="23389">
-      <OrphaCode>439755</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439755</ExpertLink>
-      <Name lang="nl">Polyarteriitis nodosa van een enkel orgaan</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="23386">
-      <OrphaCode>439729</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439729</ExpertLink>
-      <Name lang="nl">Cutane polyarteriitis nodosa</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="23387">
-      <OrphaCode>439737</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439737</ExpertLink>
-      <Name lang="nl">Primaire polyarteriitis nodosa</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
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-    <Disorder id="23384">
-      <OrphaCode>439246</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439246</ExpertLink>
-      <Name lang="nl">ABèta2M-amyloïdose</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="23385">
-      <OrphaCode>439254</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439254</ExpertLink>
-      <Name lang="nl">ITM2B-amyloïdose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="23397">
-      <OrphaCode>440221</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=440221</ExpertLink>
-      <Name lang="nl">Congenitale paralyse van nervus oculomotorius</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="23398">
-      <OrphaCode>440233</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=440233</ExpertLink>
-      <Name lang="nl">Congenitale paralyse van nervus abducens</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
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-    <Disorder id="23393">
-      <OrphaCode>439854</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439854</ExpertLink>
-      <Name lang="nl">Fatale congenitale hypertrofische cardiomyopathie als gevolg van glycogeenstapelingsziekte</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="23392">
-      <OrphaCode>439849</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439849</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve ernstige congenitale neutropenie</Name>
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-        <Name lang="nl">Categorie</Name>
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-      <OrphaCode>439897</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439897</ExpertLink>
-      <Name lang="nl">Letale foetale cerebrale-renale-urogenitale agenesie/hypoplasie-syndroom</Name>
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-      <OrphaCode>439881</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=439881</ExpertLink>
-      <Name lang="nl">Plastische bronchitis</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Interstitiële longziekte door ABCA3-deficiëntie</Name>
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-      <Name lang="nl">Interstitiële longziekte door SP-C-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <Name lang="nl">Necrotiserende infectie van weke delen</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=441452</ExpertLink>
-      <Name lang="nl">Lamellair cataract met vroege aanvang</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=440987</ExpertLink>
-      <Name lang="nl">Geïsoleerde agenesie van galblaas</Name>
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-      <Name lang="nl">Autosomaal dominante spastische paraplegie type 9B</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23120">
-      <OrphaCode>420702</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420702</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve ernstige congenitale neutropenie door CSF3R-deficiëntie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23121">
-      <OrphaCode>420728</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420728</ExpertLink>
-      <Name lang="nl">Gecombineerde oxidatieve fosforylatiedeficiëntie type 20</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="23122">
-      <OrphaCode>420733</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420733</ExpertLink>
-      <Name lang="nl">Gecombineerde oxidatieve fosforylatiedeficiëntie type 21</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="23123">
-      <OrphaCode>420741</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420741</ExpertLink>
-      <Name lang="nl">RIDDLE-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-    <Disorder id="23109">
-      <OrphaCode>420492</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420492</ExpertLink>
-      <Name lang="nl">Cervicale dystonie met aanvang op volwassen leeftijd, DYT23-type</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="23108">
-      <OrphaCode>420485</OrphaCode>
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-      <Name lang="nl">Cranio-cervicale dystonie met betrokkenheid van larynx en bovenste ledematen</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-    <Disorder id="23111">
-      <OrphaCode>420556</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420556</ExpertLink>
-      <Name lang="nl">Visual snow-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="23104">
-      <OrphaCode>420402</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420402</ExpertLink>
-      <Name lang="nl">Dehiscentie van canalis semicircularis-syndroom</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Glycogeenstapelingsziekte door zure-maltasedeficiëntie, late aanvang</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <AverageAgeOfOnset id="23536">
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-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="23117">
-      <OrphaCode>420611</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420611</ExpertLink>
-      <Name lang="nl">Voorbijgaand myeloproliferatief syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420584</ExpertLink>
-      <Name lang="nl">Postaxiale polydactylie - anomalieën van adenohypofyse - faciale dysmorfie-syndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-    <Disorder id="23119">
-      <OrphaCode>420699</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=420699</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve ernstige congenitale neutropenie door CXCR2-deficiëntie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423306</ExpertLink>
-      <Name lang="nl">Microcefalie - kleine gestalte - intellectuele achterstand - faciale dysmorfie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23166">
-      <OrphaCode>423717</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423717</ExpertLink>
-      <Name lang="nl">Cutane larva migrans</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="23164">
-      <OrphaCode>423693</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423693</ExpertLink>
-      <Name lang="nl">Rechterventrikel met dubbele uitstroom met subaortaal of doubly-committed ventrikelseptumdefect</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
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-    <Disorder id="23165">
-      <OrphaCode>423712</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423712</ExpertLink>
-      <Name lang="nl">Rechterventrikel met dubbele uitstroom met atrioventriculair septumdefect, pulmonalisklepstenose, heterotaxie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
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-    <Disorder id="23160">
-      <OrphaCode>423479</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423479</ExpertLink>
-      <Name lang="nl">X-gebonden intellectuele achterstand - spasticiteit van ledemaat - retinadystrofie - deficiëntie van arginine-vasopressine-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="23161">
-      <OrphaCode>423655</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423655</ExpertLink>
-      <Name lang="nl">ARX-gerelateerd encefalopathie - hersenmalformatie-spectrum</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="23138">
-      <OrphaCode>422526</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=422526</ExpertLink>
-      <Name lang="nl">Erfelijk heldercellig niercelcarcinoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="23151">
-      <OrphaCode>423275</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423275</ExpertLink>
-      <Name lang="nl">Spinocerebellaire ataxie type 40</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="23193">
-      <OrphaCode>424065</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424065</ExpertLink>
-      <Name lang="nl">Solide pseudopapillair carcinoom van pancreas</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="23192">
-      <OrphaCode>424058</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424058</ExpertLink>
-      <Name lang="nl">Intraductaal papillair mucineus carcinoom van pancreas</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="23195">
-      <OrphaCode>424080</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424080</ExpertLink>
-      <Name lang="nl">Ongedifferentieerd carcinoom met osteoclastachtige reuscellen van pancreas</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="23194">
-      <OrphaCode>424073</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424073</ExpertLink>
-      <Name lang="nl">Sereus cystadenocarcinoom van prancreas</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="23197">
-      <OrphaCode>424107</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424107</ExpertLink>
-      <Name lang="nl">Congenitale myopathie met myasthenie-achtige aanvang</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23196">
-      <OrphaCode>424099</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424099</ExpertLink>
-      <Name lang="nl">Colobomateuze microftalmie - rhizomele dysplasie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23198">
-      <OrphaCode>424261</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424261</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve limb-girdle-spierdystrofie type 2Y</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="23185">
-      <OrphaCode>424016</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424016</ExpertLink>
-      <Name lang="nl">Adenocarcinoom van anaal kanaal</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="23187">
-      <OrphaCode>424027</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424027</ExpertLink>
-      <Name lang="nl">Progressieve myoclonische epilepsie type 8</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
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-    <Disorder id="23186">
-      <OrphaCode>424019</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424019</ExpertLink>
-      <Name lang="nl">Plaveiselcelcarcinoom van anaal kanaal</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
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-    <Disorder id="23189">
-      <OrphaCode>424039</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424039</ExpertLink>
-      <Name lang="nl">Plaveiselcelcarcinoom van pancreas</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
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-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="23191">
-      <OrphaCode>424053</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424053</ExpertLink>
-      <Name lang="nl">Mucineus cystadenocarcinoom van pancreas</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="23190">
-      <OrphaCode>424046</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424046</ExpertLink>
-      <Name lang="nl">Acinuscelcarcinoom van pancreas</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="23176">
-      <OrphaCode>423968</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423968</ExpertLink>
-      <Name lang="nl">Plaveiselcelcarcinoom van dunne darm</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="23180">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=423994</ExpertLink>
-      <Name lang="nl">Plaveiselcelcarcinoom van colon</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="23182">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=424002</ExpertLink>
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-      <OrphaCode>505227</OrphaCode>
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-      <Name lang="nl">Gecombineerde immuundeficiëntie door GINS1-deficiëntie</Name>
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-      <OrphaCode>505237</OrphaCode>
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-      <Name lang="nl">Vroeg aanvangende insulten - distale ledemaatanomalieën - faciale dysmorfie - globale ontwikkelingsachterstand-syndroom</Name>
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-      <OrphaCode>588</OrphaCode>
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-      <Name lang="nl">Spier-oog-hersenziekte</Name>
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-      <OrphaCode>899</OrphaCode>
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-      <Name lang="nl">Syndroom van Walker-Warburg</Name>
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-      <Name lang="nl">3-methylglutaconacidurie type 9</Name>
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-    <Disorder id="25849">
-      <OrphaCode>496790</OrphaCode>
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-      <Name lang="nl">Oculaire anomalieën - axonale neuropathie - ontwikkelingsachterstand-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="25674">
-      <OrphaCode>494433</OrphaCode>
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-      <Name lang="nl">MIRAGE-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="25675">
-      <OrphaCode>494439</OrphaCode>
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-      <Name lang="nl">Retinitis pigmentosa - gehoorverlies - hypothyreoïdie - vroegtijdige veroudering - faciale dysmorfie-syndroom</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="25672">
-      <OrphaCode>494424</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494424</ExpertLink>
-      <Name lang="nl">Extracraniële halsslagader-aneurysma</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="25673">
-      <OrphaCode>494428</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494428</ExpertLink>
-      <Name lang="nl">Idiopathische pleuroparenchymale fibro-elastose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="25678">
-      <OrphaCode>494451</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494451</ExpertLink>
-      <Name lang="nl">Basaalcelcarcinoom van vulva</Name>
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-        <Name lang="nl">Histopathologisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="25679">
-      <OrphaCode>494454</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494454</ExpertLink>
-      <Name lang="nl">Adenocarcinoom van vulva</Name>
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-        <Name lang="nl">Histopathologisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="25676">
-      <OrphaCode>494444</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494444</ExpertLink>
-      <Name lang="nl">DIAPH1-gerelateerd sensorineuraal gehoorverlies - trombocytopenie-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="25677">
-      <OrphaCode>494448</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494448</ExpertLink>
-      <Name lang="nl">Plaveiselcelcarcinoom van vulva</Name>
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-        <Name lang="nl">Histopathologisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="25667">
-      <OrphaCode>494344</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494344</ExpertLink>
-      <Name lang="nl">RERE-gerelateerd neurologische ontwikkelingssyndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="25670">
-      <OrphaCode>494418</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494418</ExpertLink>
-      <Name lang="nl">Vulvacarcinoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494421</ExpertLink>
-      <Name lang="nl">Sacrococcygeaal teratoom</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494547</ExpertLink>
-      <Name lang="nl">Plaveiselcelcarcinoom van hypofarynx</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-      <Name lang="nl">Goedaardige chorea - striatale betrokkenheid-syndroom met aanvang in de kindertijd</Name>
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-      <OrphaCode>494526</OrphaCode>
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-      <Name lang="nl">Gegeneraliseerde dyskinesie met orofaciale betrokkenheid met aanvang in de zuigelingentijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=494550</ExpertLink>
-      <Name lang="nl">Plaveiselcelcarcinoom van larynx</Name>
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-      <OrphaCode>500180</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=500180</ExpertLink>
-      <Name lang="nl">Motorische en cognitieve regressie syndroom met aanvang in de kindertijd en met extrapiramidale bewegingsstoornis</Name>
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-    <Disorder id="26005">
-      <OrphaCode>500188</OrphaCode>
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-      <Name lang="nl">X-gebonden atresie van uitwendige gehoorgang - wijde inwendige gehoorgang - faciale dysmorfie-syndroom</Name>
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-      <Name lang="nl">Q-koorts</Name>
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-      <Name lang="nl">Hersenmalformaties - musculoskeletale afwijkingen - faciale dysmorfie - intellectuele achterstand-syndroom</Name>
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-      <Name lang="nl">Microcefalie - hypoplasie van corpus callosum en vermis cerebelli - faciale dysmorfie - intellectuele achterstand-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=505</ExpertLink>
-      <Name lang="nl">Syndroom van Graham Little-Piccardi-Lassueur</Name>
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-      <Name lang="nl">Folliculitis decalvans van Quinquaud</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=222</ExpertLink>
-      <Name lang="nl">Erosieve pustuleuze dermatose van schedelhuid</Name>
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-      <OrphaCode>170</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=170</ExpertLink>
-      <Name lang="nl">Wollig haar</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>500548</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=500548</ExpertLink>
-      <Name lang="nl">Osteosclerotische metafysaire dysplasie</Name>
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-      <OrphaCode>169</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=169</ExpertLink>
-      <Name lang="nl">Ringed hair-ziekte</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=500533</ExpertLink>
-      <Name lang="nl">Polyhydramnion - megalencefalie - symptomatische epilepsie-syndroom</Name>
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-      <OrphaCode>168</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=168</ExpertLink>
-      <Name lang="nl">Loose anagen-syndroom</Name>
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-      <OrphaCode>500545</OrphaCode>
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-      <Name lang="nl">Ernstige neurologische ontwikkelingsstoornissen met voedingsproblemen - stereotiepe handbewegingen - bilateraal cataract</Name>
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-      <OrphaCode>345</OrphaCode>
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-      <Name lang="nl">Dissecerende cellulitis van hoofdhuid</Name>
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-      <Name lang="nl">Plaveiselcelcarcinoom van lip</Name>
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-      <Name lang="nl">Mitochondriale myopathie - cerebellaire ataxie - pigmentretinopathie-syndroom</Name>
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-      <Name lang="nl">Syndroom van Weiss-Kruszka</Name>
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-      <Name lang="nl">STAG1-gerelateerde intellectuele achterstand - faciale dysmorfie - gastro-oesofageale reflux-syndroom</Name>
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-      <OrphaCode>502437</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=502437</ExpertLink>
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-      <Name lang="nl">Erythema multiforme major</Name>
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-      <Name lang="nl">Alkalisch ceramidase 3-deficiëntie</Name>
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-      <Name lang="nl">Menstruatiecyclus-afhankelijke periodieke koorts</Name>
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-      <Name lang="nl">Ziekte van Gorham-Stout</Name>
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-      <OrphaCode>728</OrphaCode>
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-    <Disorder id="25928">
-      <OrphaCode>498497</OrphaCode>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=720</ExpertLink>
-      <Name lang="nl">Pili bifurcati</Name>
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-      <Name lang="nl">Primaire cutis verticis gyrata</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-      <Name lang="nl">Trichofolliculoom</Name>
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-      <OrphaCode>498602</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=498602</ExpertLink>
-      <Name lang="nl">Brachydactylie van Sugarman</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>247</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=247</ExpertLink>
-      <Name lang="nl">Erfelijke aritmogene cardiomyopathie</Name>
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-      <OrphaCode>498693</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=498693</ExpertLink>
-      <Name lang="nl">MYBPC1-gerelateerd autosomaal recessief niet-letaal arthrogryposis multiplex congenita-syndroom</Name>
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-      <OrphaCode>444</OrphaCode>
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-      <Name lang="nl">Erfelijke hypotrichose, Marie Unna-type</Name>
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-      <Name lang="nl">Verworven hypertrichosis lanuginosa</Name>
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-      <Name lang="nl">Hyaliene fibromatose syndroom</Name>
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-      <Name lang="nl">Prolifererende trichilemmale cyste</Name>
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-      <Name lang="nl">LRP5-gerelateerde primaire osteoporose</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="8624">
-      <OrphaCode>38</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=38</ExpertLink>
-      <Name lang="nl">Acrokerato-elastoïdosis van Costa</Name>
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-        <Name lang="nl">Ziekte</Name>
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-    <Disorder id="8625">
-      <OrphaCode>39</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=39</ExpertLink>
-      <Name lang="nl">Acromelanosis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="8630">
-      <OrphaCode>241</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=241</ExpertLink>
-      <Name lang="nl">Dyschromatosis universalis hereditaria</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="8631">
-      <OrphaCode>316</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=316</ExpertLink>
-      <Name lang="nl">Erytrokeratodermia progressiva symmetrica</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="8629">
-      <OrphaCode>211</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=211</ExpertLink>
-      <Name lang="nl">Familiale cylindromatose</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-    <Disorder id="8618">
-      <OrphaCode>658</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=658</ExpertLink>
-      <Name lang="nl">Niet-histamine-geïnduceerd angio-oedeem</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="8617">
-      <OrphaCode>3282</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=3282</ExpertLink>
-      <Name lang="nl">Multifocale atriumtachycardie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="8616">
-      <OrphaCode>188</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=188</ExpertLink>
-      <Name lang="nl">Systemisch capillair leksyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-      <OrphaCode>303</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=303</ExpertLink>
-      <Name lang="nl">Dystrofische epidermolysis bullosa</Name>
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-        <AverageAgeOfOnset id="23515">
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-      <OrphaCode>305</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=305</ExpertLink>
-      <Name lang="nl">Junctionele epidermolysis bullosa</Name>
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-        <Name lang="nl">Group of phenomes</Name>
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-      <Name lang="nl">Ulerythema ophryogenes</Name>
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-      <Name lang="nl">Letaal non-compactie van linkerventrikel - insulten - hypotonie - cataract - ontwikkelingsachterstand-syndroom</Name>
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-      <OrphaCode>478664</OrphaCode>
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-      <Name lang="nl">Erfelijke sensorische en autonome neuropathie type 8</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>477650</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=477650</ExpertLink>
-      <Name lang="nl">Fibroblastische reuma</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <Name lang="nl">IL-21-gerelateerde infantiele inflammatoire darmziekte</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <OrphaCode>477684</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=477684</ExpertLink>
-      <Name lang="nl">Gecombineerde oxidatieve fosforylatiedeficiëntie type 26</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      <OrphaCode>477673</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=477673</ExpertLink>
-      <Name lang="nl">Postnatale microcefalie - infantiele hypotonie - spastische diplegie - dysartrie - intellectuele achterstand-syndroom</Name>
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-      <OrphaCode>477738</OrphaCode>
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-      <Name lang="nl">Pediatrische multipele sclerose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <Name lang="nl">Pontiene autosomaal dominante microangiopathie met leuko-encefalopathie</Name>
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-      <Name lang="nl">Nodulaire fasciitis</Name>
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-      <OrphaCode>477774</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=477774</ExpertLink>
-      <Name lang="nl">Gecombineerde oxidatieve fosforylatiedeficiëntie type 27</Name>
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-      <OrphaCode>476119</OrphaCode>
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-      <Name lang="nl">Autosomaal dominant preaxiale polydactylie - hypertrichose van bovenrug-syndroom</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=476113</ExpertLink>
-      <Name lang="nl">Gecombineerde immuundeficiëntie door TFRC-deficiëntie</Name>
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-      <OrphaCode>476126</OrphaCode>
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-      <Name lang="nl">Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome</Name>
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-      <Name lang="nl">Congenitale gegeneraliseerde hypercontractiele spierstijfheid-syndroom</Name>
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-      <OrphaCode>70590</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70590</ExpertLink>
-      <Name lang="nl">Infantiele apneu</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10966">
-      <OrphaCode>70595</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70595</ExpertLink>
-      <Name lang="nl">Sensorische ataxische neuropathie - dysartrie - oftalmoparese-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10967">
-      <OrphaCode>70596</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70596</ExpertLink>
-      <Name lang="nl">Congenitale infectie met Epstein-Barrvirus</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10964">
-      <OrphaCode>70593</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70593</ExpertLink>
-      <Name lang="nl">Immuundeficiëntie door selectieve deficiëntie van antipolysacharide-antilichaam</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="3">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10965">
-      <OrphaCode>70594</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70594</ExpertLink>
-      <Name lang="nl">Doparesponsieve dystonie als gevolg van sepiapterinereductasedeficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10954">
-      <OrphaCode>70578</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70578</ExpertLink>
-      <Name lang="nl">Acuut ademhalingsnoodsyndroom bij volwassenen</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10953">
-      <OrphaCode>70573</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70573</ExpertLink>
-      <Name lang="nl">Kleincellige longkanker</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10952">
-      <OrphaCode>70568</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70568</ExpertLink>
-      <Name lang="nl">Post-transplantatie lymfoproliferatieve aandoening</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10959">
-      <OrphaCode>70588</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70588</ExpertLink>
-      <Name lang="nl">Meconiumaspiratiesyndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10945">
-      <OrphaCode>70472</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70472</ExpertLink>
-      <Name lang="nl">Congenitale lactaatacidose, Saguenay-Lac-Saint-Jean-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10951">
-      <OrphaCode>70567</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70567</ExpertLink>
-      <Name lang="nl">Cholangiocarcinoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10950">
-      <OrphaCode>70482</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70482</ExpertLink>
-      <Name lang="nl">Carcinoom van oesofagus</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10949">
-      <OrphaCode>70476</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70476</ExpertLink>
-      <Name lang="nl">Vernale keratoconjunctivitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10948">
-      <OrphaCode>70475</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=70475</ExpertLink>
-      <Name lang="nl">Radiatieproctitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10941">
-      <OrphaCode>69744</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69744</ExpertLink>
-      <Name lang="nl">Circumscripte palmoplantaire hypokeratose</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10942">
-      <OrphaCode>69745</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69745</ExpertLink>
-      <Name lang="nl">Wratachtig dyskeratoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10936">
-      <OrphaCode>69735</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69735</ExpertLink>
-      <Name lang="nl">Hypotrichose - lymfoedeem - teleangiëctasie - renaal defect-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10937">
-      <OrphaCode>69736</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69736</ExpertLink>
-      <Name lang="nl">Bilaterale acute irisdepigmentatie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10938">
-      <OrphaCode>69737</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69737</ExpertLink>
-      <Name lang="nl">Syndroom van Bosley-Salih-Alorainy</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10939">
-      <OrphaCode>69739</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69739</ExpertLink>
-      <Name lang="nl">Athabaskan-hersenstamdysgenesiesyndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10932">
-      <OrphaCode>69663</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69663</ExpertLink>
-      <Name lang="nl">Cholelithiase geassocieerd met laag gehalte aan fosfolipiden</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10933">
-      <OrphaCode>69665</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69665</ExpertLink>
-      <Name lang="nl">Intrahepatische zwangerschapscholestase</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10935">
-      <OrphaCode>69723</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69723</ExpertLink>
-      <Name lang="nl">Tyrosinemie type 3</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10924">
-      <OrphaCode>69126</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69126</ExpertLink>
-      <Name lang="nl">PAPA-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="10921">
-      <OrphaCode>69087</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69087</ExpertLink>
-      <Name lang="nl">Syndroom van Naegeli-Franceschetti-Jadassohn</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10923">
-      <OrphaCode>69125</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69125</ExpertLink>
-      <Name lang="nl">Anonychie met flexurale pigmentatie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10922">
-      <OrphaCode>69088</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69088</ExpertLink>
-      <Name lang="nl">Anhidrotische ectodermale dysplasie - immuundeficiëntie - osteopetrose - lymfoedeem-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10917">
-      <OrphaCode>69083</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69083</ExpertLink>
-      <Name lang="nl">Ectodermale dysplasie met natale tanden, Turnpenny-type</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10916">
-      <OrphaCode>69082</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69082</ExpertLink>
-      <Name lang="nl">Odonto-tricho-unguaal-digito-palmair syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10919">
-      <OrphaCode>69085</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69085</ExpertLink>
-      <Name lang="nl">Ledemaat-borstsyndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10918">
-      <OrphaCode>69084</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69084</ExpertLink>
-      <Name lang="nl">Zuivere ectodermale dysplasie van haar en nagel</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10913">
-      <OrphaCode>69077</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69077</ExpertLink>
-      <Name lang="nl">Rhabdoïde tumor</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10912">
-      <OrphaCode>69076</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69076</ExpertLink>
-      <Name lang="nl">Familiale renale glucosurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10914">
-      <OrphaCode>69078</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69078</ExpertLink>
-      <Name lang="nl">Liposarcoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10910">
-      <OrphaCode>69061</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69061</ExpertLink>
-      <Name lang="nl">Idiopathisch steroïdgevoelig nefrotisch syndroom</Name>
-      <DisorderType id="21422">
-        <Name lang="nl">Klinisch syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10911">
-      <OrphaCode>69063</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69063</ExpertLink>
-      <Name lang="nl">Congenitale membraneuze nefropathie door foetomaternale anti-neutrale endopeptidase-allo-immunisatie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10908">
-      <OrphaCode>67048</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67048</ExpertLink>
-      <Name lang="nl">3-methylglutaconacidurie type 4</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10909">
-      <OrphaCode>69028</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=69028</ExpertLink>
-      <Name lang="nl">Dysostose met brachydactylie</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="3">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="10906">
-      <OrphaCode>67046</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67046</ExpertLink>
-      <Name lang="nl">3-methylglutaconacidurie type 1</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="10907">
-      <OrphaCode>67047</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67047</ExpertLink>
-      <Name lang="nl">3-methylglutaconacidurie type 3</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10904">
-      <OrphaCode>67044</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67044</ExpertLink>
-      <Name lang="nl">Trombocytopenie met congenitale dyserytropoëtische anemie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="10905">
-      <OrphaCode>67045</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67045</ExpertLink>
-      <Name lang="nl">X-gebonden intellectuele achterstand met geïsoleerde groeihormoondeficiëntie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="10902">
-      <OrphaCode>67042</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67042</ExpertLink>
-      <Name lang="nl">Retinadegeneratie met late aanvang</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
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-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-      </AverageAgeOfOnsetList>
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-        <TypeOfInheritance id="23410">
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-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10903">
-      <OrphaCode>67043</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67043</ExpertLink>
-      <Name lang="nl">Amoebische keratitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        </TypeOfInheritance>
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-    <Disorder id="10900">
-      <OrphaCode>67039</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=67039</ExpertLink>
-      <Name lang="nl">Segmentale odontomaxillaire dysplasie</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <Name lang="nl">Extracutaan mastocytoom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64754</ExpertLink>
-      <Name lang="nl">Nevus comedonicus-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <OrphaCode>562528</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=562528</ExpertLink>
-      <Name lang="nl">Congenitale contracturen van ledematen en gelaat - hypotonie - ontwikkelingsachterstand-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="10859">
-      <OrphaCode>64755</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64755</ExpertLink>
-      <Name lang="nl">Naevus van Becker-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="28333">
-      <OrphaCode>562559</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=562559</ExpertLink>
-      <Name lang="nl">Anterieure maxillaire protrusie - strabisme - intellectuele achterstand-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="28332">
-      <OrphaCode>562538</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=562538</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve extraorale halitose</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <OrphaCode>562569</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=562569</ExpertLink>
-      <Name lang="nl">TMEM94-geassocieerd congenitaal hartdefect - faciale dysmorfie - ontwikkelingsachterstand-syndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="10835">
-      <OrphaCode>64686</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64686</ExpertLink>
-      <Name lang="nl">Syndroom van Tolosa-Hunt</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="10833">
-      <OrphaCode>64542</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64542</ExpertLink>
-      <Name lang="nl">Acrofaciale dysostose, Kennedy-Teebi-type</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="10832">
-      <OrphaCode>64280</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64280</ExpertLink>
-      <Name lang="nl">Absence-epilepsie in de kindertijd</Name>
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-        <Name lang="nl">Ziekte</Name>
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-    <Disorder id="10839">
-      <OrphaCode>64722</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64722</ExpertLink>
-      <Name lang="nl">Granulomateuze mastitis</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="10838">
-      <OrphaCode>64720</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64720</ExpertLink>
-      <Name lang="nl">Leiomyosarcoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-      <OrphaCode>64694</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=64694</ExpertLink>
-      <Name lang="nl">Loopgravenkoorts</Name>
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-      <Name lang="nl">Infectie door Bartonella bacilliformis</Name>
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-      <Name lang="nl">Iridocorneaal endotheliaal syndroom</Name>
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-      <Name lang="nl">Engelvormige falango-epifysaire dysplasie</Name>
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-      <Name lang="nl">Syndroom van Loeys-Dietz</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=59315</ExpertLink>
-      <Name lang="nl">Rombencefalosynapsis</Name>
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-      <OrphaCode>60014</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=60014</ExpertLink>
-      <Name lang="nl">Argyrie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="10774">
-      <OrphaCode>57196</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=57196</ExpertLink>
-      <Name lang="nl">Mediale condenserende osteïtis van clavicula</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="28372">
-      <OrphaCode>563690</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=563690</ExpertLink>
-      <Name lang="nl">Furunculaire myiasis door Cordylobia rodhaini</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="28373">
-      <OrphaCode>563708</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=563708</ExpertLink>
-      <Name lang="nl">Syndromale congenitale natriumdiarree</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="10771">
-      <OrphaCode>57145</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=57145</ExpertLink>
-      <Name lang="nl">SUNCT-syndroom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      <OrphaCode>563684</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=563684</ExpertLink>
-      <Name lang="nl">Furunculaire myiasis door Dermatobia hominis</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="28371">
-      <OrphaCode>563687</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=563687</ExpertLink>
-      <Name lang="nl">Furunculaire myiasis door Cordylobia anthropophaga</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="10770">
-      <OrphaCode>56970</OrphaCode>
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-      <Name lang="nl">Mucineus cystadenoom in de kindertijd</Name>
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-      <Name lang="nl">Koude agglutinine-ziekte</Name>
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-        <Name lang="nl">Histopathologisch subtype</Name>
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-      <OrphaCode>563666</OrphaCode>
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-      <Name lang="nl">Sereus cystadenoom in de kindertijd</Name>
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-      <Name lang="nl">Geïsoleerde exencefalie</Name>
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-      <Name lang="nl">Geïsoleerde anencefalie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23508">
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-      <Name lang="nl">Carcinoom van galblaas en extrahepatische galwegen</Name>
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-      <OrphaCode>563589</OrphaCode>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <Name lang="nl">Subtype van aandoening</Name>
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-      <Name lang="nl">Chondrosarcoom</Name>
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-      <Name lang="nl">Auto-immune hepatitis type 2</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=55881</ExpertLink>
-      <Name lang="nl">Adamantinoom</Name>
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-      <Name lang="nl">Hypotrichosis simplex</Name>
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-      <Name lang="nl">Craniosynostose - microretrognathie - ernstige intellectuele achterstand-syndroom</Name>
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-      <Name lang="nl">Resistentie tegen thyroïdhormoon door een mutatie in thyroïdhormoonreceptor-alfa</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="11148">
-      <OrphaCode>79106</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79106</ExpertLink>
-      <Name lang="nl">Syndroom van Eiken</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="28494">
-      <OrphaCode>566243</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=566243</ExpertLink>
-      <Name lang="nl">Resistentie tegen thyroïdhormoon door een mutatie in thyroïdhormoonreceptor-bèta</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="11151">
-      <OrphaCode>79118</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79118</ExpertLink>
-      <Name lang="nl">Neonatale diabetes - congenitale hypothyreoïdie - congenitaal glaucoom - hepatische fibrose - polycystische nieren</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="28495">
-      <OrphaCode>566393</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=566393</ExpertLink>
-      <Name lang="nl">Acute mestcelleukemie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11150">
-      <OrphaCode>79113</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79113</ExpertLink>
-      <Name lang="nl">Mandibulofaciale dysostose - microcefalie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11144">
-      <OrphaCode>79102</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79102</ExpertLink>
-      <Name lang="nl">Thyreotoxische periodieke paralyse</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11147">
-      <OrphaCode>79105</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79105</ExpertLink>
-      <Name lang="nl">Myxofibrosarcoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11141">
-      <OrphaCode>79099</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79099</ExpertLink>
-      <Name lang="nl">Interstitiële granulomateuze dermatitis met artritis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11140">
-      <OrphaCode>79098</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79098</ExpertLink>
-      <Name lang="nl">Sympathische oftalmie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11143">
-      <OrphaCode>79101</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79101</ExpertLink>
-      <Name lang="nl">Hyperprolinemie type 2</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="28487">
-      <OrphaCode>566192</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=566192</ExpertLink>
-      <Name lang="nl">Congenitale autosmaal recessieve trombocytopenie met kleine bloedplaatjes</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11142">
-      <OrphaCode>79100</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79100</ExpertLink>
-      <Name lang="nl">Atrophoderma vermiculata</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11137">
-      <OrphaCode>79095</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79095</ExpertLink>
-      <Name lang="nl">Congenitaal defect van galzuursynthese type 4</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="11136">
-      <OrphaCode>79094</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79094</ExpertLink>
-      <Name lang="nl">Syndroom van Grange</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="28482">
-      <OrphaCode>566175</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=566175</ExpertLink>
-      <Name lang="nl">Hyperactivatie van complementsysteem - angiopathische trombose - proteïneverliezende enteropathie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11139">
-      <OrphaCode>79097</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79097</ExpertLink>
-      <Name lang="nl">Folinezuurresponsieve insulten</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    </Disorder>
-    <Disorder id="11138">
-      <OrphaCode>79096</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79096</ExpertLink>
-      <Name lang="nl">Pyridoxaalfosfaatresponsieve insulten</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    </Disorder>
-    <Disorder id="11164">
-      <OrphaCode>79138</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79138</ExpertLink>
-      <Name lang="nl">Bickerstaff-hersenstamencefalitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
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-    </Disorder>
-    <Disorder id="11165">
-      <OrphaCode>79139</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79139</ExpertLink>
-      <Name lang="nl">Japanse encefalitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="11166">
-      <OrphaCode>79140</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79140</ExpertLink>
-      <Name lang="nl">Cutaan neuro-endocrien carcinoom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-    <Disorder id="11167">
-      <OrphaCode>79141</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79141</ExpertLink>
-      <Name lang="nl">Erfelijke pijnlijke eeltplekken</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
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-    <Disorder id="11160">
-      <OrphaCode>79134</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79134</ExpertLink>
-      <Name lang="nl">DEND-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11161">
-      <OrphaCode>79135</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79135</ExpertLink>
-      <Name lang="nl">Episodische ataxie type 3</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="11162">
-      <OrphaCode>79136</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79136</ExpertLink>
-      <Name lang="nl">Episodische ataxie type 4</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="11163">
-      <OrphaCode>79137</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79137</ExpertLink>
-      <Name lang="nl">Gegeneraliseerde epilepsie - paroxysmale dyskinesie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11156">
-      <OrphaCode>79129</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79129</ExpertLink>
-      <Name lang="nl">Trichodysplasie - amelogenesis imperfecta-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11159">
-      <OrphaCode>79133</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79133</ExpertLink>
-      <Name lang="nl">Focale faciale dermale dysplasie type I</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11152">
-      <OrphaCode>79124</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79124</ExpertLink>
-      <Name lang="nl">Hepatische veno-occlusieve ziekte - immuundeficiëntie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="28496">
-      <OrphaCode>566396</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=566396</ExpertLink>
-      <Name lang="nl">Chronische mestcelleukemie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11153">
-      <OrphaCode>79126</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79126</ExpertLink>
-      <Name lang="nl">Acute interstitiële pneumonie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="11154">
-      <OrphaCode>79127</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79127</ExpertLink>
-      <Name lang="nl">Respiratoire bronchiolitis - interstitiële longziekte-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11155">
-      <OrphaCode>79128</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=79128</ExpertLink>
-      <Name lang="nl">Lymfoïde interstitiële pneumonie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11106">
-      <OrphaCode>77293</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77293</ExpertLink>
-      <Name lang="nl">Chronische viscerale deficiëntie van zure sfingomyelinase</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="11107">
-      <OrphaCode>77295</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77295</ExpertLink>
-      <Name lang="nl">Odontoleukodystrofie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    <Disorder id="11104">
-      <OrphaCode>77261</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77261</ExpertLink>
-      <Name lang="nl">Ziekte van Gaucher type 3</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11105">
-      <OrphaCode>77292</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77292</ExpertLink>
-      <Name lang="nl">Infantiele neuroviscerale deficiëntie van zure sfingomyelinase</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>77298</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77298</ExpertLink>
-      <Name lang="nl">Anoftalmie/microftalmie - oesofageale atresie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77299</ExpertLink>
-      <Name lang="nl">Microftalmie - hersenatrofie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
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-      <OrphaCode>77296</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77296</ExpertLink>
-      <Name lang="nl">Syndroom van Morgagni-Stewart-Morel</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77297</ExpertLink>
-      <Name lang="nl">Syndroom van Majeed</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <OrphaCode>567502</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=567502</ExpertLink>
-      <Name lang="nl">B-cel-immuundeficiëntie - ledemaatanomalieën - urogenitale malformaties-syndroom</Name>
-      <DisorderType id="21394">
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="11112">
-      <OrphaCode>77300</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77300</ExpertLink>
-      <Name lang="nl">Auriculaire abnormaliteiten - gespleten lip met of zonder gespleten verhemelte - oculaire abnormaliteiten</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23480">
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-    <Disorder id="11113">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=77301</ExpertLink>
-      <Name lang="nl">Monosomie 9q22.3-syndroom</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=567550</ExpertLink>
-      <Name lang="nl">Idiopathisch multidrugresistent nefrotisch syndroom</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      <Name lang="nl">Idiopathisch steroïdresistent nefrotisch syndroom met sensitiviteit voor immuunsuppressieve tweedelijnsbehandeling</Name>
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-      <Name lang="nl">Nefrotisch syndroom zonder extrarenale manifestaties</Name>
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-      <Name lang="nl">PPARG-gerelateerde familiale partiële lipodystrofie</Name>
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-      <OrphaCode>79078</OrphaCode>
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-      <Name lang="nl">IgG4-gerelateerde dacryoadenitis en sialoadenitis</Name>
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-      <Name lang="nl">Juveniele polyposis beginnend in de zuigelingentijd</Name>
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-      <Name lang="nl">Verworven partiële lipodystrofie</Name>
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-      <Name lang="nl">Verworven gegeneraliseerde lipodystrofie</Name>
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-      <OrphaCode>79084</OrphaCode>
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-    <Disorder id="28552">
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-      <Name lang="nl">Parodontaal syndroom van Ehlers-Danlos</Name>
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-    <Disorder id="11083">
-      <OrphaCode>75496</OrphaCode>
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-      <Name lang="nl">B4GALT7-gerelateerd spondylodysplastisch syndroom van Ehlers-Danlos</Name>
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-      <OrphaCode>75497</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=75497</ExpertLink>
-      <Name lang="nl">X-gebonden syndroom van Ehlers-Danlos</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-    <Disorder id="11086">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=75508</ExpertLink>
-      <Name lang="nl">Angio-osteohypotrofisch syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="11087">
-      <OrphaCode>75563</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=75563</ExpertLink>
-      <Name lang="nl">X-gebonden sideroblastische anemie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Syndroom van Mueller-Weiss</Name>
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-        <Name lang="nl">Aandoening</Name>
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-    <Disorder id="11089">
-      <OrphaCode>75565</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=75565</ExpertLink>
-      <Name lang="nl">Tropische endomyocardfibrose</Name>
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-      <OrphaCode>75564</OrphaCode>
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-      <Name lang="nl">Verworven idiopathische sideroblastische anemie</Name>
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-    <Disorder id="11091">
-      <OrphaCode>75567</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=75567</ExpertLink>
-      <Name lang="nl">Primaire progressieve bevroren gang</Name>
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-        <TypeOfInheritance id="23480">
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-    <Disorder id="11090">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=75566</ExpertLink>
-      <Name lang="nl">Loeffler-endocarditis</Name>
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-      <Name lang="nl">Nanoftalmie</Name>
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-      <Name lang="nl">Distale deletie 1q-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10421">
-      <OrphaCode>36383</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36383</ExpertLink>
-      <Name lang="nl">COL4A1/2-gerelateerde familiale vasculaire leuko-encefalopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="0">
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10423">
-      <OrphaCode>36386</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36386</ExpertLink>
-      <Name lang="nl">Erfelijke sensorische en autonome neuropathie type 1</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10409">
-      <OrphaCode>36234</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36234</ExpertLink>
-      <Name lang="nl">Bacteriële toxischeshocksyndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10411">
-      <OrphaCode>36236</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36236</ExpertLink>
-      <Name lang="nl">Staphylococcal scalded skin-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10410">
-      <OrphaCode>36235</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36235</ExpertLink>
-      <Name lang="nl">Roodvonk door stafylokok</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10413">
-      <OrphaCode>36238</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36238</ExpertLink>
-      <Name lang="nl">Door stafylokokken veroorzaakte necrotiserende pneumonie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10412">
-      <OrphaCode>36237</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36237</ExpertLink>
-      <Name lang="nl">Bulleuze impetigo</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
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-    <Disorder id="10415">
-      <OrphaCode>36273</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36273</ExpertLink>
-      <Name lang="nl">Linitis plastica van maag</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10414">
-      <OrphaCode>36258</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36258</ExpertLink>
-      <Name lang="nl">Ziekte van Buerger</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="10401">
-      <OrphaCode>35808</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=35808</ExpertLink>
-      <Name lang="nl">Maligne sex cord-stromale tumor van ovarium</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
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-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="10400">
-      <OrphaCode>35807</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=35807</ExpertLink>
-      <Name lang="nl">Maligne kiemceltumor van ovarium</Name>
-      <DisorderType id="36561">
-        <Name lang="nl">Categorie</Name>
-      </DisorderType>
-      <DisorderGroup id="36540">
-        <Name lang="nl">Groep van aandoeningen</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="5">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23480">
-          <Name lang="nl">Unknown</Name>
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-    <Disorder id="10403">
-      <OrphaCode>35878</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=35878</ExpertLink>
-      <Name lang="nl">Hyperinsulinisme - hyperammoniëmie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="10402">
-      <OrphaCode>35858</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=35858</ExpertLink>
-      <Name lang="nl">Syndroom van Imerslund-Gräsbeck</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <TypeOfInheritance id="23417">
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-    <Disorder id="10405">
-      <OrphaCode>35909</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=35909</ExpertLink>
-      <Name lang="nl">Gecombineerde deficiëntie van factor V en factor VIII</Name>
-      <DisorderType id="21394">
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-      </DisorderType>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
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-    <Disorder id="10404">
-      <OrphaCode>35889</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=35889</ExpertLink>
-      <Name lang="nl">Acute intoxicatie door opioïd</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-        <TypeOfInheritance id="23494">
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-    <Disorder id="10407">
-      <OrphaCode>36204</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=36204</ExpertLink>
-      <Name lang="nl">Intestinale lymfangiëctasie</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
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-    <Disorder id="10406">
-      <OrphaCode>35981</OrphaCode>
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-      <Name lang="nl">Polymicrogyrie</Name>
-      <DisorderType id="21436">
-        <Name lang="nl">Group of phenomes</Name>
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-        <AverageAgeOfOnset id="23529">
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>33572</OrphaCode>
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-      <Name lang="nl">Deficiëntie van 5-oxoprolinase</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      <Name lang="nl">Meningokokkenmeningitis</Name>
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-      <Name lang="nl">Bulleuze lichen planus</Name>
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-      <OrphaCode>33402</OrphaCode>
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-      <Name lang="nl">Pediatrisch hepatocellulair carcinoom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=34217</ExpertLink>
-      <Name lang="nl">Ziekte van Naxos</Name>
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-      <OrphaCode>34149</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=34149</ExpertLink>
-      <Name lang="nl">Autosomaal dominante tubulo-interstitiële nierziekte</Name>
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-          <Name lang="nl">Autosomaal dominant</Name>
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-      <OrphaCode>33577</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=33577</ExpertLink>
-      <Name lang="nl">Nodulaire niet-suppuratieve panniculitis</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="10329">
-      <OrphaCode>33574</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=33574</ExpertLink>
-      <Name lang="nl">Deficiëntie van glutamaat-cysteïneligase</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-      <OrphaCode>33573</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=33573</ExpertLink>
-      <Name lang="nl">Deficiëntie van gamma-glutamyltranspeptidase</Name>
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-      <OrphaCode>33110</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=33110</ExpertLink>
-      <Name lang="nl">Autosomale niet-syndromale agammaglobulinemie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=33111</ExpertLink>
-      <Name lang="nl">Granulomateuze slappe huid</Name>
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-      <Name lang="nl">Letaal multipele pterygium-syndroom</Name>
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-      <OrphaCode>33067</OrphaCode>
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-      <Name lang="nl">Metafysaire chondrodysplasie, Jansen-type</Name>
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-      <Name lang="nl">NAD(P)HX-epimerasedeficiëntie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=555437</ExpertLink>
-      <Name lang="nl">Lymfoplasmacytaire inflammatoire pseudotumor van lever</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-    <Disorder id="28118">
-      <OrphaCode>555874</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=555874</ExpertLink>
-      <Name lang="nl">Congenitale dysplasie van tricuspidalisklep</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <OrphaCode>555877</OrphaCode>
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-      <Name lang="nl">FLNA-gerelateerde X-gebonden myxomateuze klepdysplasie</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <Name lang="nl">IgA-pemfigus</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <Name lang="nl">Familiaal hypoaldosteronisme met vroege aanvang</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <AverageAgeOfOnset id="23522">
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-          <Name lang="nl">Neonataal</Name>
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-      <OrphaCode>556037</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=556037</ExpertLink>
-      <Name lang="nl">Familiaal hypoaldosteronisme met late aanvang</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-          <Name lang="nl">Volwassenheid</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-      <OrphaCode>556985</OrphaCode>
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-      <Name lang="nl">Vroeg aanvangende calcificerende leuko-encefalopathie - skeletdysplasie</Name>
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-      <OrphaCode>556955</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=556955</ExpertLink>
-      <Name lang="nl">Agenesie van pancreas - holoprosencefalie-syndroom</Name>
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-          <Name lang="nl">Antenataal</Name>
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-      <Name lang="nl">Neonatale epileptische encefalopathie door glutaminasedeficiëntie</Name>
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-      <OrphaCode>557056</OrphaCode>
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-      <Name lang="nl">Spastische ataxie-dysartrie door glutaminasedeficiëntie</Name>
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-      <Name lang="nl">Oculoskeletodentaal syndroom</Name>
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-    <Disorder id="11960">
-      <OrphaCode>90069</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90069</ExpertLink>
-      <Name lang="nl">Systemische monochloroacetaatvergiftiging</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11941">
-      <OrphaCode>90050</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90050</ExpertLink>
-      <Name lang="nl">Prematurenretinopathie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11940">
-      <OrphaCode>90045</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90045</ExpertLink>
-      <Name lang="nl">Erfelijke malabsorptie van folaat</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11943">
-      <OrphaCode>90052</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90052</ExpertLink>
-      <Name lang="nl">Terugkerende hepatitis C-virus-geïnduceerde leverziekte bij levertransplantaatrecipiënten</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11942">
-      <OrphaCode>90051</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90051</ExpertLink>
-      <Name lang="nl">Sepsis bij premature zuigeling</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11937">
-      <OrphaCode>90041</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90041</ExpertLink>
-      <Name lang="nl">Syndroom van Gaisböck</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11936">
-      <OrphaCode>90039</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90039</ExpertLink>
-      <Name lang="nl">Hemoglobine D-ziekte</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11939">
-      <OrphaCode>90044</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90044</ExpertLink>
-      <Name lang="nl">Familiale pseudohyperkaliëmie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11938">
-      <OrphaCode>90042</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90042</ExpertLink>
-      <Name lang="nl">Primaire familiale polycytemie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11949">
-      <OrphaCode>90058</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90058</ExpertLink>
-      <Name lang="nl">Ruggenmergletsel</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11951">
-      <OrphaCode>90060</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90060</ExpertLink>
-      <Name lang="nl">Diffuse alveolaire hemorragie</Name>
-      <DisorderType id="21422">
-        <Name lang="nl">Klinisch syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="5">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11950">
-      <OrphaCode>90059</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90059</ExpertLink>
-      <Name lang="nl">Plotseling sensorineuraal gehoorverlies</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11944">
-      <OrphaCode>90053</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90053</ExpertLink>
-      <Name lang="nl">Complicaties na hematopoëtische stamceltransplantatie</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11947">
-      <OrphaCode>90056</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90056</ExpertLink>
-      <Name lang="nl">Matig en ernstig traumatisch hersenletsel</Name>
-      <DisorderType id="21429">
-        <Name lang="nl">Particulaire klinische situatie binnen een ziekte of syndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11926">
-      <OrphaCode>90024</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90024</ExpertLink>
-      <Name lang="nl">Doofheid met aplasie van labyrint, microtie en microdontie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11925">
-      <OrphaCode>90023</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90023</ExpertLink>
-      <Name lang="nl">Primair immuundeficiëntiesyndroom door P14/LAMTOR2-deficiëntie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11921">
-      <OrphaCode>90003</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90003</ExpertLink>
-      <Name lang="nl">Inflammatoire pseudotumor van lever</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11934">
-      <OrphaCode>90037</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90037</ExpertLink>
-      <Name lang="nl">Medicatiegeïnduceerde auto-immune hemolytische anemie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11935">
-      <OrphaCode>90038</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90038</ExpertLink>
-      <Name lang="nl">Shigatoxine-geassocieerd hemolytisch-uremisch syndroom</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
-      </DisorderType>
-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11932">
-      <OrphaCode>90035</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90035</ExpertLink>
-      <Name lang="nl">Paroxysmale koude hemoglobinurie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11933">
-      <OrphaCode>90036</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90036</ExpertLink>
-      <Name lang="nl">Auto-immune hemolytische anemie, gemengd type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11930">
-      <OrphaCode>90031</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90031</ExpertLink>
-      <Name lang="nl">Niet-sferocytische hemolytische anemie door deficiëntie van hexokinase</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11931">
-      <OrphaCode>90033</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90033</ExpertLink>
-      <Name lang="nl">Auto-immune hemolytische anemie, warmte-type</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23424">
-          <Name lang="nl">Multigeen/multifactorieel</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="11928">
-      <OrphaCode>90026</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90026</ExpertLink>
-      <Name lang="nl">Primaire erytromelalgie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <TypeOfInheritance id="23410">
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-    <Disorder id="11929">
-      <OrphaCode>90030</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90030</ExpertLink>
-      <Name lang="nl">Hemolytische anemie door deficiëntie van glutathionreductase</Name>
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-    <Disorder id="11911">
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-      <Name lang="nl">X-gebonden hypofosfatemie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-    <Disorder id="11909">
-      <OrphaCode>89844</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=89844</ExpertLink>
-      <Name lang="nl">Lissencefalie-syndroom, Norman-Roberts-type</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-    <Disorder id="11908">
-      <OrphaCode>89843</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=89843</ExpertLink>
-      <Name lang="nl">Dystrofische epidermolysis bullosa pruriginosa</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11907">
-      <OrphaCode>89842</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=89842</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve gegeneraliseerde dystrofische epidermolysis bullosa, intermediaire vorm</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Neonataal</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11919">
-      <OrphaCode>90001</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90001</ExpertLink>
-      <Name lang="nl">X-gebonden kegeldisfunctiesyndroom met myopie</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90000</ExpertLink>
-      <Name lang="nl">Erythema elevatum diutinum</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=89938</ExpertLink>
-      <Name lang="nl">Syndroom van Bartter type 4</Name>
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-    <Disorder id="11912">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=89937</ExpertLink>
-      <Name lang="nl">Autosomaal dominante hypofosfatemische rachitis</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90340</ExpertLink>
-      <Name lang="nl">Blausyndroom</Name>
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-      <Name lang="nl">Xeroderma pigmentosum, variante vorm</Name>
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-    <Disorder id="12009">
-      <OrphaCode>90322</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90322</ExpertLink>
-      <Name lang="nl">Syndroom van Cockayne type 2</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="12008">
-      <OrphaCode>90321</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90321</ExpertLink>
-      <Name lang="nl">Syndroom van Cockayne type 1</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="12010">
-      <OrphaCode>90324</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90324</ExpertLink>
-      <Name lang="nl">Syndroom van Cockayne type 3</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11986">
-      <OrphaCode>90156</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90156</ExpertLink>
-      <Name lang="nl">Centrifugale lipodystrofie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="5">
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="11987">
-      <OrphaCode>90157</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90157</ExpertLink>
-      <Name lang="nl">Medicatiegeïnduceerde gelokaliseerde lipodystrofie</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="0">
-      </TypeOfInheritanceList>
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-    <Disorder id="11984">
-      <OrphaCode>90153</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90153</ExpertLink>
-      <Name lang="nl">Mandibuloacrale dysplasie met lipodystrofie type A</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11985">
-      <OrphaCode>90154</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90154</ExpertLink>
-      <Name lang="nl">Mandibuloacrale dysplasie met type B-lipodystrofie</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11990">
-      <OrphaCode>90160</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90160</ExpertLink>
-      <Name lang="nl">Drukgeïnduceerde gelokaliseerde lipoatrofie</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Op leeftijd</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="11988">
-      <OrphaCode>90158</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90158</ExpertLink>
-      <Name lang="nl">Idiopathische gelokaliseerde lipodystrofie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="0">
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-    <Disorder id="11989">
-      <OrphaCode>90159</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90159</ExpertLink>
-      <Name lang="nl">Panniculitis-geïnduceerde gelokaliseerde lipodystrofie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="11994">
-      <OrphaCode>90280</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90280</ExpertLink>
-      <Name lang="nl">Chilblain lupus</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="5">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-      <Name lang="nl">Discoïde lupus erythematosus</Name>
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-    <Disorder id="11993">
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-      <Name lang="nl">Ziekte van Meige</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90285</ExpertLink>
-      <Name lang="nl">Lupus erythematosus panniculitis</Name>
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-    <Disorder id="11997">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90283</ExpertLink>
-      <Name lang="nl">Lupus erythematosus tumidus</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90080</ExpertLink>
-      <Name lang="nl">Littekenvorming bij filtrerende glaucoomchirurgie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90078</ExpertLink>
-      <Name lang="nl">Invasieve infecties als gevolg van vancomycineresistente enterokokken</Name>
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-      <Name lang="nl">Ziekte van Charcot-Marie-Tooth - doofheid - intellectuele achterstand-syndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=514980</ExpertLink>
-      <Name lang="nl">ATP13A2-gerelateerd parkinsonisme</Name>
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-      <OrphaCode>90081</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90081</ExpertLink>
-      <Name lang="nl">AIDS-cachexiesyndroom</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90118</ExpertLink>
-      <Name lang="nl">Ernstige axonale neuropathie met vroege aanvang door MFN2-deficiëntie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=90117</ExpertLink>
-      <Name lang="nl">Hereditaire motorische en sensorische neuropathie, Okinawa-type</Name>
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-      <Name lang="nl">Pediatrische ziekte van Graves</Name>
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-      <Name lang="nl">Pediatrisch glaucoom</Name>
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-      <OrphaCode>88673</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=88673</ExpertLink>
-      <Name lang="nl">Hepatocellulair carcinoom</Name>
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-      <Name lang="nl">Autosomaal recessieve ataxie, Beauce-type</Name>
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-      <OrphaCode>88659</OrphaCode>
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-      <Name lang="nl">Autosomaal dominante progressieve nefropathie met hypertensie</Name>
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-      <Name lang="nl">Amelogenesis imperfecta</Name>
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-      <Name lang="nl">Familiale acute necrotiserende encefalopathie</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="11805">
-      <OrphaCode>88618</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=88618</ExpertLink>
-      <Name lang="nl">Deficiëntie van S-adenosylhomocysteïnehydrolase</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11804">
-      <OrphaCode>88616</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=88616</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve niet-syndromale intellectuele achterstand</Name>
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-        <Name lang="nl">Etiologisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11802">
-      <OrphaCode>87884</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=87884</ExpertLink>
-      <Name lang="nl">Niet-syndromale genetische doofheid</Name>
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-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-        <TypeOfInheritance id="23431">
-          <Name lang="nl">X-gebonden recessief</Name>
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-    <Disorder id="11801">
-      <OrphaCode>87876</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=87876</ExpertLink>
-      <Name lang="nl">Sialidose type 2</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="4">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11800">
-      <OrphaCode>87503</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=87503</ExpertLink>
-      <Name lang="nl">Mal de Meleda</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11793">
-      <OrphaCode>86920</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86920</ExpertLink>
-      <Name lang="nl">Dermatopathia pigmentosa reticularis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="11792">
-      <OrphaCode>86919</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86919</ExpertLink>
-      <Name lang="nl">Keratosis palmaris et plantaris - clinodactylie-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="11791">
-      <OrphaCode>86918</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86918</ExpertLink>
-      <Name lang="nl">Diffuse palmoplantaire keratodermie - acrocyanose-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="11788">
-      <OrphaCode>86915</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86915</ExpertLink>
-      <Name lang="nl">Lymfoedeem - atriumseptumdefecten - veranderingen in aangezicht-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="27340">
-      <OrphaCode>522077</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=522077</ExpertLink>
-      <Name lang="nl">Infantiele hypotonie - oculomotorische anomalieën - hyperkinetische bewegingen - ontwikkelingsachterstand-syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="11786">
-      <OrphaCode>86913</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86913</ExpertLink>
-      <Name lang="nl">Myoclonische epilepsie bij niet-progressieve encefalopathieën</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="11787">
-      <OrphaCode>86914</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86914</ExpertLink>
-      <Name lang="nl">Lymfoedeem - cerebrale arterioveneuze anomalie - primaire pulmonale hypertensie-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-    <Disorder id="11784">
-      <OrphaCode>86909</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86909</ExpertLink>
-      <Name lang="nl">Myoclonische epilepsie in de kinderjaren</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="11785">
-      <OrphaCode>86911</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86911</ExpertLink>
-      <Name lang="nl">Epilepsie met myoclonische absences</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-    <Disorder id="27333">
-      <OrphaCode>521450</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=521450</ExpertLink>
-      <Name lang="nl">LAMA5-gerelateerd multisystemisch syndroom</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="27332">
-      <OrphaCode>521445</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=521445</ExpertLink>
-      <Name lang="nl">Microcefalie - faciale dysmorfie - oculaire anomalieën - multipele congenitale anomalieën-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-    <Disorder id="27331">
-      <OrphaCode>521438</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=521438</ExpertLink>
-      <Name lang="nl">Congenitale vertebrale-cardiale-renale anomalieën-syndroom</Name>
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-        <Name lang="nl">Malformatiesyndroom</Name>
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-    <Disorder id="11778">
-      <OrphaCode>86900</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86900</ExpertLink>
-      <Name lang="nl">Sarcoom van interdigiterende dendritische cellen</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <Name lang="nl">Congenitaal cataract - ernstige neonatale hepatopathie - algehele ontwikkelingsachterstand-syndroom</Name>
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-      <OrphaCode>86902</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=86902</ExpertLink>
-      <Name lang="nl">Folliculaire dendritische celsarcoom</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-      <OrphaCode>93262</OrphaCode>
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-      <OrphaCode>93269</OrphaCode>
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-      <Name lang="nl">Klaverbladschedel - multipele congenitale anomalieën-syndroom</Name>
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-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
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-    </Disorder>
-    <Disorder id="12160">
-      <OrphaCode>91547</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=91547</ExpertLink>
-      <Name lang="nl">Terugkerende koorts</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="12163">
-      <OrphaCode>93100</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93100</ExpertLink>
-      <Name lang="nl">Agenesie van nier, unilateraal</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="27458">
-      <OrphaCode>527468</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=527468</ExpertLink>
-      <Name lang="nl">Hernia diaphragmatica - korte darm - asplenie-syndroom</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="12162">
-      <OrphaCode>92050</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=92050</ExpertLink>
-      <Name lang="nl">Congenitale tufting-enteropathie</Name>
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-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
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-    <Disorder id="12173">
-      <OrphaCode>93160</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93160</ExpertLink>
-      <Name lang="nl">Hypocalciëmische vitamine D-resistente rachitis</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="12174">
-      <OrphaCode>93164</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93164</ExpertLink>
-      <Name lang="nl">Transiënt pseudohypoaldosteronisme</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
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-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
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-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-      </TypeOfInheritanceList>
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-    <Disorder id="12169">
-      <OrphaCode>93114</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93114</ExpertLink>
-      <Name lang="nl">Autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type E</Name>
-      <DisorderType id="21394">
-        <Name lang="nl">Ziekte</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23564">
-          <Name lang="nl">No data available</Name>
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-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="2">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="12168">
-      <OrphaCode>93111</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93111</ExpertLink>
-      <Name lang="nl">HNF1B-gerelateerde autosomaal dominante tubulo-interstitiële nierziekte</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <AverageAgeOfOnsetList count="6">
-        <AverageAgeOfOnset id="23536">
-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23508">
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
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-    <Disorder id="12170">
-      <OrphaCode>93126</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93126</ExpertLink>
-      <Name lang="nl">Pauci-immune glomerulonefritis</Name>
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-        <Name lang="nl">Ziekte</Name>
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-        <Name lang="nl">Aandoening</Name>
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-          <Name lang="nl">Puber</Name>
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-        <AverageAgeOfOnset id="23543">
-          <Name lang="nl">Volwassenheid</Name>
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-        <AverageAgeOfOnset id="23529">
-          <Name lang="nl">Kindertijd</Name>
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-        <AverageAgeOfOnset id="23550">
-          <Name lang="nl">Op leeftijd</Name>
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-        <TypeOfInheritance id="23494">
-          <Name lang="nl">Niet toepasbaar</Name>
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-    <Disorder id="12177">
-      <OrphaCode>93172</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93172</ExpertLink>
-      <Name lang="nl">Renale dysplasie, unilateraal</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23557">
-          <Name lang="nl">Elke leeftijd</Name>
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-    <Disorder id="12178">
-      <OrphaCode>93173</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93173</ExpertLink>
-      <Name lang="nl">Renale dysplasie, bilateraal</Name>
-      <DisorderType id="21450">
-        <Name lang="nl">Klinisch subtype</Name>
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-      <DisorderGroup id="36554">
-        <Name lang="nl">Subtype van aandoening</Name>
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-          <Name lang="nl">Elke leeftijd</Name>
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-      <OrphaCode>93322</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93322</ExpertLink>
-      <Name lang="nl">Geïsoleerde hemimelie van tibia</Name>
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-        <Name lang="nl">Morfologische anomalie</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93321</ExpertLink>
-      <Name lang="nl">Geïsoleerde hemimelie van radius</Name>
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-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93325</ExpertLink>
-      <Name lang="nl">Autosomaal dominant Kenny-Caffeysyndroom</Name>
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-        <AverageAgeOfOnset id="23529">
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93323</ExpertLink>
-      <Name lang="nl">Geïsoleerde hemimelie van fibula</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93329</ExpertLink>
-      <Name lang="nl">Autosomaal recessieve omodysplasie</Name>
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-        <Name lang="nl">Klinisch subtype</Name>
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-        <AverageAgeOfOnset id="23522">
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-          <Name lang="nl">Neonataal</Name>
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-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
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-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93336</ExpertLink>
-      <Name lang="nl">Polydactylie van trifalangeale duim</Name>
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-      <Name lang="nl">Postaxiale polydactylie type B</Name>
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-    <Disorder id="12269">
-      <OrphaCode>93334</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93334</ExpertLink>
-      <Name lang="nl">Postaxiale polydactylie type A</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="1">
-        <AverageAgeOfOnset id="23508">
-          <Name lang="nl">Antenataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="12268">
-      <OrphaCode>93333</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93333</ExpertLink>
-      <Name lang="nl">Pelviscapulaire dysplasie</Name>
-      <DisorderType id="21401">
-        <Name lang="nl">Malformatiesyndroom</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23417">
-          <Name lang="nl">Autosomaal recessief</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="12274">
-      <OrphaCode>93339</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93339</ExpertLink>
-      <Name lang="nl">Polydactylie van bifalangeale duim en/of hallux</Name>
-      <DisorderType id="21415">
-        <Name lang="nl">Morfologische anomalie</Name>
-      </DisorderType>
-      <DisorderGroup id="36547">
-        <Name lang="nl">Aandoening</Name>
-      </DisorderGroup>
-      <AverageAgeOfOnsetList count="2">
-        <AverageAgeOfOnset id="23522">
-          <Name lang="nl">Kindsheid</Name>
-        </AverageAgeOfOnset>
-        <AverageAgeOfOnset id="23515">
-          <Name lang="nl">Neonataal</Name>
-        </AverageAgeOfOnset>
-      </AverageAgeOfOnsetList>
-      <TypeOfInheritanceList count="1">
-        <TypeOfInheritance id="23410">
-          <Name lang="nl">Autosomaal dominant</Name>
-        </TypeOfInheritance>
-      </TypeOfInheritanceList>
-    </Disorder>
-    <Disorder id="12272">
-      <OrphaCode>93337</OrphaCode>
-      <ExpertLink lang="nl">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=nl&amp;Expert=93337</ExpertLink>
-      <Name lang="nl">Polydactylie van wijsvinger</Name>
-      <Disorder