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                        <Name lang="en">Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome</Name>
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                            <Name lang="en">Ellis Van Creveld syndrome</Name>
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                            <Name lang="en">Cranioectodermal dysplasia</Name>
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                            <Name lang="en">Short rib-polydactyly syndrome, Beemer-Langer type</Name>
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                              <Name lang="en">Malformation syndrome</Name>
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                            <Name lang="en">Short rib-polydactyly syndrome, Majewski type</Name>
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                            <Name lang="en">Short rib-polydactyly syndrome, Saldino-Noonan type</Name>
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                              <Name lang="en">Malformation syndrome</Name>
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                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93271</ExpertLink>
                            <Name lang="en">Short rib-polydactyly syndrome, Verma-Naumoff type</Name>
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                              <Name lang="en">Malformation syndrome</Name>
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                            <OrphaCode>397715</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=397715</ExpertLink>
                            <Name lang="en">Joubert syndrome with Jeune asphyxiating thoracic dystrophy</Name>
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                              <Name lang="en">Malformation syndrome</Name>
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                            <OrphaCode>498497</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=498497</ExpertLink>
                            <Name lang="en">Short rib-polydactyly syndrome type 5</Name>
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                              <Name lang="en">Malformation syndrome</Name>
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                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=957</ExpertLink>
                        <Name lang="en">Acropectorovertebral dysplasia</Name>
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                        <Name lang="en">Fetal akinesia deformation sequence</Name>
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                        <Name lang="en">Lethal congenital contracture syndrome type 1</Name>
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                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1838">
                        <OrphaCode>1861</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1861</ExpertLink>
                        <Name lang="en">Thoracic dysplasia-hydrocephalus syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1951">
                        <OrphaCode>2017</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2017</ExpertLink>
                        <Name lang="en">Sternal cleft</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2222">
                        <OrphaCode>2391</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2391</ExpertLink>
                        <Name lang="en">Congenitally short costocoracoid ligament</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2283">
                        <OrphaCode>2470</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2470</ExpertLink>
                        <Name lang="en">Matthew-Wood syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2509">
                        <OrphaCode>2753</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2753</ExpertLink>
                        <Name lang="en">Orofaciodigital syndrome type 4</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2853">
                        <OrphaCode>3181</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3181</ExpertLink>
                        <Name lang="en">Sprengel deformity</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2947">
                        <OrphaCode>3317</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3317</ExpertLink>
                        <Name lang="en">Thoracolaryngopelvic dysplasia</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="11038">
                        <OrphaCode>73230</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=73230</ExpertLink>
                        <Name lang="en">Ossification anomalies-psychomotor developmental delay syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="24023">
                        <OrphaCode>464366</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=464366</ExpertLink>
                        <Name lang="en">NEK9-related lethal skeletal dysplasia</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18216">
                    <OrphaCode>182111</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182111</ExpertLink>
                    <Name lang="en">Respiratory malformation</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="27">
                    <ClassificationNode>
                      <Disorder id="14100">
                        <OrphaCode>99083</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99083</ExpertLink>
                        <Name lang="en">Pulmonary artery hypoplasia</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3459">
                        <OrphaCode>3188</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3188</ExpertLink>
                        <Name lang="en">Congenital pulmonary veins atresia or stenosis</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="14143">
                            <OrphaCode>99126</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99126</ExpertLink>
                            <Name lang="en">Congenital pulmonary vein atresia</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="31729">
                            <OrphaCode>642071</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=642071</ExpertLink>
                            <Name lang="en">Primary pulmonary vein stenosis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3462">
                        <OrphaCode>185</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=185</ExpertLink>
                        <Name lang="en">Scimitar syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="534">
                        <OrphaCode>2414</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2414</ExpertLink>
                        <Name lang="en">Congenital pulmonary lymphangiectasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="538">
                        <OrphaCode>2444</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2444</ExpertLink>
                        <Name lang="en">Congenital pulmonary airway malformation</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="20506">
                            <OrphaCode>280827</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280827</ExpertLink>
                            <Name lang="en">Congenital pulmonary airway malformation type 0</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20507">
                            <OrphaCode>280832</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280832</ExpertLink>
                            <Name lang="en">Congenital pulmonary airway malformation type 1</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20508">
                            <OrphaCode>280840</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280840</ExpertLink>
                            <Name lang="en">Congenital pulmonary airway malformation type 2</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20509">
                            <OrphaCode>280847</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280847</ExpertLink>
                            <Name lang="en">Congenital pulmonary airway malformation type 3</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20510">
                            <OrphaCode>280854</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280854</ExpertLink>
                            <Name lang="en">Congenital pulmonary airway malformation type 4</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="597">
                        <OrphaCode>3346</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3346</ExpertLink>
                        <Name lang="en">Tracheal agenesis</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="715">
                        <OrphaCode>984</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=984</ExpertLink>
                        <Name lang="en">Pulmonary agenesis</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="798">
                        <OrphaCode>2040</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2040</ExpertLink>
                        <Name lang="en">Congenital respiratory-biliary fistula</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="802">
                        <OrphaCode>1928</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1928</ExpertLink>
                        <Name lang="en">Congenital lobar emphysema</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1400">
                        <OrphaCode>1120</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1120</ExpertLink>
                        <Name lang="en">Lung agenesis-heart defect-thumb anomalies syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1941">
                        <OrphaCode>2004</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2004</ExpertLink>
                        <Name lang="en">Laryngotracheoesophageal cleft</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="12498">
                            <OrphaCode>93938</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93938</ExpertLink>
                            <Name lang="en">Laryngotracheoesophageal cleft type 1</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12499">
                            <OrphaCode>93939</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93939</ExpertLink>
                            <Name lang="en">Laryngotracheoesophageal cleft type 2</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12500">
                            <OrphaCode>93940</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93940</ExpertLink>
                            <Name lang="en">Laryngotracheoesophageal cleft type 3</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12501">
                            <OrphaCode>93941</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93941</ExpertLink>
                            <Name lang="en">Laryngotracheoesophageal cleft type 4</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20437">
                            <OrphaCode>280205</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280205</ExpertLink>
                            <Name lang="en">Laryngotracheoesophageal cleft type 0</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2125">
                        <OrphaCode>2257</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2257</ExpertLink>
                        <Name lang="en">Primary pulmonary hypoplasia</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2233">
                        <OrphaCode>2407</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2407</ExpertLink>
                        <Name lang="en">Laryngo-onycho-cutaneous syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2283">
                        <OrphaCode>2470</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2470</ExpertLink>
                        <Name lang="en">Matthew-Wood syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2729">
                        <OrphaCode>3035</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3035</ExpertLink>
                        <Name lang="en">Growth delay-hydrocephaly-lung hypoplasia syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2947">
                        <OrphaCode>3317</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3317</ExpertLink>
                        <Name lang="en">Thoracolaryngopelvic dysplasia</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3428">
                        <OrphaCode>1132</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1132</ExpertLink>
                        <Name lang="en">Aortic arch defects</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="7">
                        <ClassificationNode>
                          <Disorder id="14092">
                            <OrphaCode>99075</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99075</ExpertLink>
                            <Name lang="en">Encircling double aortic arch</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14093">
                            <OrphaCode>99076</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99076</ExpertLink>
                            <Name lang="en">Persistent fifth aortic arch</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14094">
                            <OrphaCode>99077</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99077</ExpertLink>
                            <Name lang="en">Kommerell diverticulum</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14095">
                            <OrphaCode>99078</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99078</ExpertLink>
                            <Name lang="en">Neuhauser anomaly</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14096">
                            <OrphaCode>99079</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99079</ExpertLink>
                            <Name lang="en">Cervical aortic arch</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14098">
                            <OrphaCode>99081</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99081</ExpertLink>
                            <Name lang="en">Right aortic arch</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14099">
                            <OrphaCode>99082</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99082</ExpertLink>
                            <Name lang="en">Dysphagia lusoria</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3457">
                        <OrphaCode>3161</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3161</ExpertLink>
                        <Name lang="en">Congenital pulmonary sequestration</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="20503">
                            <OrphaCode>280802</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280802</ExpertLink>
                            <Name lang="en">Intralobar congenital pulmonary sequestration</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20504">
                            <OrphaCode>280811</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280811</ExpertLink>
                            <Name lang="en">Extralobar congenital pulmonary sequestration</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20505">
                            <OrphaCode>280821</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280821</ExpertLink>
                            <Name lang="en">Communicating congenital bronchopulmonary-foregut malformation</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10960">
                        <OrphaCode>70589</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70589</ExpertLink>
                        <Name lang="en">Bronchopulmonary dysplasia</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12589">
                        <OrphaCode>95430</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95430</ExpertLink>
                        <Name lang="en">Congenital tracheomalacia</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23013">
                        <OrphaCode>411501</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=411501</ExpertLink>
                        <Name lang="en">Williams-Campbell syndrome</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31859">
                        <OrphaCode>649014</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=649014</ExpertLink>
                        <Name lang="en">Bronchial malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="4">
                        <ClassificationNode>
                          <Disorder id="31856">
                            <OrphaCode>648992</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=648992</ExpertLink>
                            <Name lang="en">Non-syndromic bridging bronchus</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="31858">
                            <OrphaCode>649010</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=649010</ExpertLink>
                            <Name lang="en">Non-syndromic congenital bronchial atresia</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="31861">
                            <OrphaCode>649029</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=649029</ExpertLink>
                            <Name lang="en">Isolated left bronchial isomerism</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="797">
                            <OrphaCode>2357</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2357</ExpertLink>
                            <Name lang="en">Bronchogenic cyst</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32457">
                        <OrphaCode>700286</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=700286</ExpertLink>
                        <Name lang="en">Congenital high airway obstruction syndrome</Name>
                        <DisorderType id="21422">
                          <Name lang="en">Clinical syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="236">
                        <OrphaCode>774</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=774</ExpertLink>
                        <Name lang="en">Hereditary hemorrhagic telangiectasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23661">
                        <OrphaCode>454750</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=454750</ExpertLink>
                        <Name lang="en">Isolated tracheoesophageal fistula</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3441">
                        <OrphaCode>2038</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2038</ExpertLink>
                        <Name lang="en">Pulmonary arteriovenous malformation</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14067">
                        <OrphaCode>99050</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99050</ExpertLink>
                        <Name lang="en">Abnormal origin of right or left pulmonary artery from the aorta</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
              </ClassificationNodeChildList>
            </ClassificationNode>
            <ClassificationNode>
              <Disorder id="13078">
                <OrphaCode>98060</OrphaCode>
                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98060</ExpertLink>
                <Name lang="en">Rare respiratory tumor</Name>
                <DisorderType id="36561">
                  <Name lang="en">Category</Name>
                </DisorderType>
              </Disorder>
              <ClassificationNodeChildList count="3">
                <ClassificationNode>
                  <Disorder id="24185">
                    <OrphaCode>466962</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=466962</ExpertLink>
                    <Name lang="en">SMARCA4-deficient sarcoma of thorax</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="1063">
                    <OrphaCode>150</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=150</ExpertLink>
                    <Name lang="en">Nasopharyngeal carcinoma</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="14881">
                    <OrphaCode>101945</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101945</ExpertLink>
                    <Name lang="en">Rare bronchopulmonary and pleural cavity tumors</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="10">
                    <ClassificationNode>
                      <Disorder id="31371">
                        <OrphaCode>617916</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=617916</ExpertLink>
                        <Name lang="en">Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="752">
                        <OrphaCode>2420</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2420</ExpertLink>
                        <Name lang="en">Primary pulmonary lymphoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10645">
                        <OrphaCode>50251</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=50251</ExpertLink>
                        <Name lang="en">Pleural mesothelioma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="32134">
                            <OrphaCode>675837</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675837</ExpertLink>
                            <Name lang="en">Diffused pleural mesothelioma</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32133">
                            <OrphaCode>675833</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675833</ExpertLink>
                            <Name lang="en">Localized pleural mesothelioma</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32135">
                            <OrphaCode>675841</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675841</ExpertLink>
                            <Name lang="en">Pleural mesothelioma in situ</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10845">
                        <OrphaCode>64741</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=64741</ExpertLink>
                        <Name lang="en">Pulmonary blastoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10846">
                        <OrphaCode>64742</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=64742</ExpertLink>
                        <Name lang="en">Pleuropulmonary blastoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="14506">
                            <OrphaCode>99933</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99933</ExpertLink>
                            <Name lang="en">Pleuropulmonary blastoma type 1</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14507">
                            <OrphaCode>99934</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99934</ExpertLink>
                            <Name lang="en">Pleuropulmonary blastoma type 2</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14508">
                            <OrphaCode>99935</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99935</ExpertLink>
                            <Name lang="en">Pleuropulmonary blastoma type 3</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20598">
                            <OrphaCode>284343</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=284343</ExpertLink>
                            <Name lang="en">DICER1 tumor-predisposition syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20601">
                            <OrphaCode>284362</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=284362</ExpertLink>
                            <Name lang="en">Fetal lung interstitial tumor</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10953">
                        <OrphaCode>70573</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70573</ExpertLink>
                        <Name lang="en">Small cell lung cancer</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12881">
                        <OrphaCode>97287</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97287</ExpertLink>
                        <Name lang="en">Bronchial neuroendocrine tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20604">
                        <OrphaCode>284395</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=284395</ExpertLink>
                        <Name lang="en">Well-differentiated fetal adenocarcinoma of the lung</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32132">
                        <OrphaCode>675822</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675822</ExpertLink>
                        <Name lang="en">Well-differentiated papillary mesothelial tumour of the pleura</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32131">
                        <OrphaCode>675814</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675814</ExpertLink>
                        <Name lang="en">Adenomatoid tumour of the pleura</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
              </ClassificationNodeChildList>
            </ClassificationNode>
            <ClassificationNode>
              <Disorder id="14880">
                <OrphaCode>101944</OrphaCode>
                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101944</ExpertLink>
                <Name lang="en">Rare pulmonary disease</Name>
                <DisorderType id="36561">
                  <Name lang="en">Category</Name>
                </DisorderType>
              </Disorder>
              <ClassificationNodeChildList count="46">
                <ClassificationNode>
                  <Disorder id="3768">
                    <OrphaCode>389</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=389</ExpertLink>
                    <Name lang="en">Langerhans cell histiocytosis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="4">
                    <ClassificationNode>
                      <Disorder id="32186">
                        <OrphaCode>687733</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687733</ExpertLink>
                        <Name lang="en">Pulmonary Langerhans cell histiocytosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32188">
                        <OrphaCode>687741</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687741</ExpertLink>
                        <Name lang="en">Multisystem Langerhans cell histiocytosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32187">
                        <OrphaCode>687738</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687738</ExpertLink>
                        <Name lang="en">Single-system multifocal Langerhans cell histiocytosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32185">
                        <OrphaCode>687730</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687730</ExpertLink>
                        <Name lang="en">Unifocal Langerhans cell histiocytosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="49">
                    <OrphaCode>586</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=586</ExpertLink>
                    <Name lang="en">Cystic fibrosis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="194">
                    <OrphaCode>60</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=60</ExpertLink>
                    <Name lang="en">Alpha-1-antitrypsin deficiency</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="506">
                    <OrphaCode>2140</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2140</ExpertLink>
                    <Name lang="en">Congenital diaphragmatic hernia</Name>
                    <DisorderType id="21415">
                      <Name lang="en">Morphological anomaly</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="564">
                    <OrphaCode>2903</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2903</ExpertLink>
                    <Name lang="en">Familial spontaneous pneumothorax</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="665">
                    <OrphaCode>244</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=244</ExpertLink>
                    <Name lang="en">Primary ciliary dyskinesia</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="744">
                    <OrphaCode>1164</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1164</ExpertLink>
                    <Name lang="en">Allergic bronchopulmonary aspergillosis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="3050">
                    <OrphaCode>3471</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3471</ExpertLink>
                    <Name lang="en">Young syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="3091">
                    <OrphaCode>3167</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3167</ExpertLink>
                    <Name lang="en">Siegler-Brewer-Carey syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="7030">
                    <OrphaCode>1303</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1303</ExpertLink>
                    <Name lang="en">Bronchiolitis obliterans</Name>
                    <DisorderType id="21436">
                      <Name lang="en">Clinical group</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="2">
                    <ClassificationNode>
                      <Disorder id="31941">
                        <OrphaCode>658602</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=658602</ExpertLink>
                        <Name lang="en">Transplant-related bronchiolitis obliterans</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31942">
                        <OrphaCode>658612</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=658612</ExpertLink>
                        <Name lang="en">Non-transplant-related bronchiolitis obliterans</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="7032">
                    <OrphaCode>3348</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3348</ExpertLink>
                    <Name lang="en">Tracheobronchopathia osteochondroplastica</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10413">
                    <OrphaCode>36238</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=36238</ExpertLink>
                    <Name lang="en">Staphylococcal necrotizing pneumonia</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10798">
                    <OrphaCode>60026</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=60026</ExpertLink>
                    <Name lang="en">Pulmonary nodular lymphoid hyperplasia</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10801">
                    <OrphaCode>60032</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=60032</ExpertLink>
                    <Name lang="en">Recurrent respiratory papillomatosis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10802">
                    <OrphaCode>60033</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=60033</ExpertLink>
                    <Name lang="en">Idiopathic bronchiectasis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10959">
                    <OrphaCode>70588</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70588</ExpertLink>
                    <Name lang="en">Meconium aspiration syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10961">
                    <OrphaCode>70590</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70590</ExpertLink>
                    <Name lang="en">Infantile apnea</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="11951">
                    <OrphaCode>90060</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90060</ExpertLink>
                    <Name lang="en">Diffuse alveolar hemorrhage</Name>
                    <DisorderType id="21422">
                      <Name lang="en">Clinical syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="12002">
                    <OrphaCode>90291</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90291</ExpertLink>
                    <Name lang="en">Systemic sclerosis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="3">
                    <ClassificationNode>
                      <Disorder id="18905">
                        <OrphaCode>220393</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=220393</ExpertLink>
                        <Name lang="en">Diffuse cutaneous systemic sclerosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18906">
                        <OrphaCode>220402</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=220402</ExpertLink>
                        <Name lang="en">Limited cutaneous systemic sclerosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18907">
                        <OrphaCode>220407</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=220407</ExpertLink>
                        <Name lang="en">Limited systemic sclerosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="3441">
                    <OrphaCode>2038</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2038</ExpertLink>
                    <Name lang="en">Pulmonary arteriovenous malformation</Name>
                    <DisorderType id="21415">
                      <Name lang="en">Morphological anomaly</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="16993">
                    <OrphaCode>140896</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=140896</ExpertLink>
                    <Name lang="en">Severe acute respiratory syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="17779">
                    <OrphaCode>168593</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168593</ExpertLink>
                    <Name lang="en">Sudden infant death-dysgenesis of the testes syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="17929">
                    <OrphaCode>171700</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171700</ExpertLink>
                    <Name lang="en">Diffuse panbronchiolitis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18013">
                    <OrphaCode>178320</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178320</ExpertLink>
                    <Name lang="en">Acute lung injury</Name>
                    <DisorderType id="21429">
                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18211">
                    <OrphaCode>182095</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182095</ExpertLink>
                    <Name lang="en">Interstitial lung disease</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="3">
                    <ClassificationNode>
                      <Disorder id="20104">
                        <OrphaCode>264656</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264656</ExpertLink>
                        <Name lang="en">Interstitial lung disease specific to childhood</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="20106">
                            <OrphaCode>264665</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264665</ExpertLink>
                            <Name lang="en">Primary interstitial lung disease specific to childhood</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="16696">
                                <OrphaCode>137631</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137631</ExpertLink>
                                <Name lang="en">Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20107">
                                <OrphaCode>264670</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264670</ExpertLink>
                                <Name lang="en">Primary interstitial lung disease specific to childhood due to alveolar structure disorder</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14622">
                                    <OrphaCode>100049</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100049</ExpertLink>
                                    <Name lang="en">Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="6">
                                    <ClassificationNode>
                                      <Disorder id="18666">
                                        <OrphaCode>209905</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=209905</ExpertLink>
                                        <Name lang="en">Brain-lung-thyroid syndrome</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="18862">
                                        <OrphaCode>217563</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217563</ExpertLink>
                                        <Name lang="en">Neonatal acute respiratory distress syndrome</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="20108">
                                        <OrphaCode>264675</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264675</ExpertLink>
                                        <Name lang="en">Hereditary pulmonary alveolar proteinosis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="23404">
                                        <OrphaCode>440402</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=440402</ExpertLink>
                                        <Name lang="en">Interstitial lung disease due to ABCA3 deficiency</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="23408">
                                        <OrphaCode>440427</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=440427</ExpertLink>
                                        <Name lang="en">Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="28746">
                                        <OrphaCode>572428</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=572428</ExpertLink>
                                        <Name lang="en">Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21219">
                                    <OrphaCode>306504</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306504</ExpertLink>
                                    <Name lang="en">Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20109">
                                <OrphaCode>264683</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264683</ExpertLink>
                                <Name lang="en">Primary interstitial lung disease specific to childhood due to alveolar vascular disorder</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="6">
                                <ClassificationNode>
                                  <Disorder id="534">
                                    <OrphaCode>2414</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2414</ExpertLink>
                                    <Name lang="en">Congenital pulmonary lymphangiectasia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="6520">
                                    <OrphaCode>662</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662</ExpertLink>
                                    <Name lang="en">Lymphedema with yellow nails</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18684">
                                    <OrphaCode>210122</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=210122</ExpertLink>
                                    <Name lang="en">Congenital alveolar capillary dysplasia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20110">
                                    <OrphaCode>264688</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264688</ExpertLink>
                                    <Name lang="en">Congenital chylothorax</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20111">
                                    <OrphaCode>264691</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264691</ExpertLink>
                                    <Name lang="en">Isolated pulmonary capillaritis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22087">
                                    <OrphaCode>352629</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=352629</ExpertLink>
                                    <Name lang="en">16q24.1 microdeletion syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20112">
                                <OrphaCode>264694</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264694</ExpertLink>
                                <Name lang="en">Interstitial lung disease specific to infancy</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="4">
                                <ClassificationNode>
                                  <Disorder id="12133">
                                    <OrphaCode>91359</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91359</ExpertLink>
                                    <Name lang="en">Chronic pneumonitis of infancy</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18860">
                                    <OrphaCode>217557</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217557</ExpertLink>
                                    <Name lang="en">Pulmonary interstitial glycogenosis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18861">
                                    <OrphaCode>217560</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217560</ExpertLink>
                                    <Name lang="en">Neuroendocrine cell hyperplasia of infancy</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="31449">
                                    <OrphaCode>621758</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=621758</ExpertLink>
                                    <Name lang="en">Fibrosis-neurodegeneration-cerebral angiomatosis syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20113">
                            <OrphaCode>264699</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264699</ExpertLink>
                            <Name lang="en">Secondary interstitial lung disease specific to childhood associated with a systemic disease</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="6">
                            <ClassificationNode>
                              <Disorder id="20114">
                                <OrphaCode>264704</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264704</ExpertLink>
                                <Name lang="en">Secondary interstitial lung disease specific to childhood associated with a connective tissue disease</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="4">
                                <ClassificationNode>
                                  <Disorder id="720">
                                    <OrphaCode>92</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=92</ExpertLink>
                                    <Name lang="en">Juvenile idiopathic arthritis</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="6">
                                    <ClassificationNode>
                                      <Disorder id="11710">
                                        <OrphaCode>85410</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85410</ExpertLink>
                                        <Name lang="en">Oligoarticular juvenile idiopathic arthritis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11711">
                                        <OrphaCode>85414</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85414</ExpertLink>
                                        <Name lang="en">Systemic-onset juvenile idiopathic arthritis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11713">
                                        <OrphaCode>85436</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85436</ExpertLink>
                                        <Name lang="en">Psoriasis-related juvenile idiopathic arthritis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11715">
                                        <OrphaCode>85438</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85438</ExpertLink>
                                        <Name lang="en">Enthesitis-related juvenile idiopathic arthritis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="12117">
                                        <OrphaCode>91140</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91140</ExpertLink>
                                        <Name lang="en">Unspecified juvenile idiopathic arthritis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="22944">
                                        <OrphaCode>404580</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404580</ExpertLink>
                                        <Name lang="en">Polyarticular juvenile idiopathic arthritis</Name>
                                        <DisorderType id="21436">
                                          <Name lang="en">Clinical group</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="11709">
                                            <OrphaCode>85408</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85408</ExpertLink>
                                            <Name lang="en">Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="11712">
                                            <OrphaCode>85435</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85435</ExpertLink>
                                            <Name lang="en">Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12394">
                                    <OrphaCode>93552</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93552</ExpertLink>
                                    <Name lang="en">Pediatric systemic lupus erythematosus</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12410">
                                    <OrphaCode>93568</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93568</ExpertLink>
                                    <Name lang="en">Juvenile polymyositis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12464">
                                    <OrphaCode>93672</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93672</ExpertLink>
                                    <Name lang="en">Juvenile dermatomyositis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20115">
                                <OrphaCode>264709</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264709</ExpertLink>
                                <Name lang="en">Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="1">
                                <ClassificationNode>
                                  <Disorder id="749">
                                    <OrphaCode>761</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=761</ExpertLink>
                                    <Name lang="en">Immunoglobulin A vasculitis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20116">
                                <OrphaCode>264714</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264714</ExpertLink>
                                <Name lang="en">Secondary interstitial lung disease specific to childhood associated with a granulomatous disease</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="176">
                                    <OrphaCode>379</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=379</ExpertLink>
                                    <Name lang="en">Chronic granulomatous disease</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12018">
                                    <OrphaCode>90340</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90340</ExpertLink>
                                    <Name lang="en">Blau syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20117">
                                <OrphaCode>264719</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264719</ExpertLink>
                                <Name lang="en">Secondary interstitial lung disease specific to childhood associated with a metabolic disease</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="3600">
                                    <OrphaCode>405</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=405</ExpertLink>
                                    <Name lang="en">Familial hypocalciuric hypercalcemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="3">
                                    <ClassificationNode>
                                      <Disorder id="12300">
                                        <OrphaCode>93372</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93372</ExpertLink>
                                        <Name lang="en">Familial hypocalciuric hypercalcemia type 1</Name>
                                        <DisorderType id="21443">
                                          <Name lang="en">Etiological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14760">
                                        <OrphaCode>101049</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101049</ExpertLink>
                                        <Name lang="en">Familial hypocalciuric hypercalcemia type 2</Name>
                                        <DisorderType id="21443">
                                          <Name lang="en">Etiological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14761">
                                        <OrphaCode>101050</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101050</ExpertLink>
                                        <Name lang="en">Familial hypocalciuric hypercalcemia type 3</Name>
                                        <DisorderType id="21443">
                                          <Name lang="en">Etiological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11103">
                                    <OrphaCode>77260</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=77260</ExpertLink>
                                    <Name lang="en">Gaucher disease type 2</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11104">
                                    <OrphaCode>77261</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=77261</ExpertLink>
                                    <Name lang="en">Gaucher disease type 3</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19195">
                                    <OrphaCode>231500</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231500</ExpertLink>
                                    <Name lang="en">Hermansky-Pudlak syndrome due to BLOC-3 deficiency</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="31389">
                                    <OrphaCode>618899</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=618899</ExpertLink>
                                    <Name lang="en">Acid sphingomyelinase deficiency</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="3">
                                    <ClassificationNode>
                                      <Disorder id="11105">
                                        <OrphaCode>77292</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=77292</ExpertLink>
                                        <Name lang="en">Infantile neurovisceral acid sphingomyelinase deficiency</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11106">
                                        <OrphaCode>77293</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=77293</ExpertLink>
                                        <Name lang="en">Chronic visceral acid sphingomyelinase deficiency</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="31388">
                                        <OrphaCode>618891</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=618891</ExpertLink>
                                        <Name lang="en">Chronic neurovisceral acid sphingomyelinase deficiency</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23481">
                                <OrphaCode>444092</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=444092</ExpertLink>
                                <Name lang="en">Autoimmune interstitial lung disease-arthritis syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="31416">
                                <OrphaCode>619367</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=619367</ExpertLink>
                                <Name lang="en">SAMD9L-associated autoinflammatory syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20119">
                        <OrphaCode>264735</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264735</ExpertLink>
                        <Name lang="en">Interstitial lung disease specific to adulthood</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="20120">
                            <OrphaCode>264740</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264740</ExpertLink>
                            <Name lang="en">Primary interstitial lung disease specific to adulthood</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="8">
                            <ClassificationNode>
                              <Disorder id="8627">
                                <OrphaCode>122</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=122</ExpertLink>
                                <Name lang="en">Birt-Hogg-Dubé syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3386">
                                <OrphaCode>538</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=538</ExpertLink>
                                <Name lang="en">Lymphangioleiomyomatosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3482">
                                <OrphaCode>747</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=747</ExpertLink>
                                <Name lang="en">Autoimmune pulmonary alveolar proteinosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10954">
                                <OrphaCode>70578</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70578</ExpertLink>
                                <Name lang="en">Adult acute respiratory distress syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13317">
                                <OrphaCode>98300</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98300</ExpertLink>
                                <Name lang="en">Idiopathic interstitial pneumonia</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="9">
                                <ClassificationNode>
                                  <Disorder id="7029">
                                    <OrphaCode>2032</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2032</ExpertLink>
                                    <Name lang="en">Idiopathic pulmonary fibrosis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="7034">
                                    <OrphaCode>1302</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1302</ExpertLink>
                                    <Name lang="en">Cryptogenic organizing pneumonia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11153">
                                    <OrphaCode>79126</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79126</ExpertLink>
                                    <Name lang="en">Acute interstitial pneumonia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11154">
                                    <OrphaCode>79127</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79127</ExpertLink>
                                    <Name lang="en">Respiratory bronchiolitis-interstitial lung disease syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11155">
                                    <OrphaCode>79128</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79128</ExpertLink>
                                    <Name lang="en">Lymphoid interstitial pneumonia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12134">
                                    <OrphaCode>91364</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91364</ExpertLink>
                                    <Name lang="en">Non-specific interstitial pneumonia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="13869">
                                    <OrphaCode>98852</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98852</ExpertLink>
                                    <Name lang="en">Desquamative interstitial pneumonia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21131">
                                    <OrphaCode>300564</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300564</ExpertLink>
                                    <Name lang="en">Combined pulmonary fibrosis-emphysema syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="25673">
                                    <OrphaCode>494428</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494428</ExpertLink>
                                    <Name lang="en">Idiopathic pleuroparenchymal fibroelastosis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18212">
                                <OrphaCode>182098</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182098</ExpertLink>
                                <Name lang="en">Pneumoconiosis</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="865">
                                    <OrphaCode>2302</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2302</ExpertLink>
                                    <Name lang="en">Asbestos intoxication</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="1061">
                                    <OrphaCode>133</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=133</ExpertLink>
                                    <Name lang="en">Chronic beryllium disease</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18687">
                                <OrphaCode>210136</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=210136</ExpertLink>
                                <Name lang="en">Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18932">
                                <OrphaCode>221043</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=221043</ExpertLink>
                                <Name lang="en">Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20121">
                            <OrphaCode>264745</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264745</ExpertLink>
                            <Name lang="en">Secondary interstitial lung disease specific to adulthood associated with a systemic disease</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="8611">
                                <OrphaCode>81</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=81</ExpertLink>
                                <Name lang="en">Antisynthetase syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="735">
                                <OrphaCode>797</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=797</ExpertLink>
                                <Name lang="en">Sarcoidosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20123">
                        <OrphaCode>264757</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264757</ExpertLink>
                        <Name lang="en">Interstitial lung disease in childhood and adulthood</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="20124">
                            <OrphaCode>264762</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264762</ExpertLink>
                            <Name lang="en">Primary interstitial lung disease in childhood and adulthood</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="14504">
                                <OrphaCode>99931</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99931</ExpertLink>
                                <Name lang="en">Idiopathic pulmonary hemosiderosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20125">
                                <OrphaCode>264930</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264930</ExpertLink>
                                <Name lang="en">Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="18863">
                                    <OrphaCode>217566</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217566</ExpertLink>
                                    <Name lang="en">Chronic respiratory distress with surfactant metabolism deficiency</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23403">
                                    <OrphaCode>440392</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=440392</ExpertLink>
                                    <Name lang="en">Interstitial lung disease due to SP-C deficiency</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20126">
                                <OrphaCode>264935</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264935</ExpertLink>
                                <Name lang="en">Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="1">
                                <ClassificationNode>
                                  <Disorder id="18213">
                                    <OrphaCode>182101</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182101</ExpertLink>
                                    <Name lang="en">Idiopathic eosinophilic pneumonia</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="7033">
                                        <OrphaCode>2902</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2902</ExpertLink>
                                        <Name lang="en">Idiopathic chronic eosinophilic pneumonia</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="8741">
                                        <OrphaCode>724</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=724</ExpertLink>
                                        <Name lang="en">Idiopathic acute eosinophilic pneumonia</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20127">
                            <OrphaCode>264944</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264944</ExpertLink>
                            <Name lang="en">Secondary interstitial lung disease in childhood and adulthood</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="5">
                            <ClassificationNode>
                              <Disorder id="14503">
                                <OrphaCode>99930</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99930</ExpertLink>
                                <Name lang="en">Secondary pulmonary hemosiderosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20128">
                                <OrphaCode>264949</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264949</ExpertLink>
                                <Name lang="en">Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="4">
                                <ClassificationNode>
                                  <Disorder id="747">
                                    <OrphaCode>375</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=375</ExpertLink>
                                    <Name lang="en">Anti-glomerular basement membrane disease</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18214">
                                    <OrphaCode>182104</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182104</ExpertLink>
                                    <Name lang="en">Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="1">
                                    <ClassificationNode>
                                      <Disorder id="3631">
                                        <OrphaCode>809</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=809</ExpertLink>
                                        <Name lang="en">Mixed connective tissue disease</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20130">
                                    <OrphaCode>264968</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264968</ExpertLink>
                                    <Name lang="en">Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="853">
                                        <OrphaCode>646</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=646</ExpertLink>
                                        <Name lang="en">Niemann-Pick disease type C</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="5">
                                        <ClassificationNode>
                                          <Disorder id="18801">
                                            <OrphaCode>216972</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=216972</ExpertLink>
                                            <Name lang="en">Niemann-Pick disease type C, severe perinatal form</Name>
                                            <DisorderType id="21450">
                                              <Name lang="en">Clinical subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18802">
                                            <OrphaCode>216975</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=216975</ExpertLink>
                                            <Name lang="en">Niemann-Pick disease type C, severe early infantile neurologic onset</Name>
                                            <DisorderType id="21450">
                                              <Name lang="en">Clinical subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18803">
                                            <OrphaCode>216978</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=216978</ExpertLink>
                                            <Name lang="en">Niemann-Pick disease type C, late infantile neurologic onset</Name>
                                            <DisorderType id="21450">
                                              <Name lang="en">Clinical subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18804">
                                            <OrphaCode>216981</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=216981</ExpertLink>
                                            <Name lang="en">Niemann-Pick disease type C, juvenile neurologic onset</Name>
                                            <DisorderType id="21450">
                                              <Name lang="en">Clinical subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18805">
                                            <OrphaCode>216986</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=216986</ExpertLink>
                                            <Name lang="en">Niemann-Pick disease type C, adult neurologic onset</Name>
                                            <DisorderType id="21450">
                                              <Name lang="en">Clinical subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11102">
                                        <OrphaCode>77259</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=77259</ExpertLink>
                                        <Name lang="en">Gaucher disease type 1</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20131">
                                    <OrphaCode>264973</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264973</ExpertLink>
                                    <Name lang="en">Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="12115">
                                        <OrphaCode>91138</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91138</ExpertLink>
                                        <Name lang="en">Cryoglobulinemic vasculitis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="12396">
                                            <OrphaCode>93554</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93554</ExpertLink>
                                            <Name lang="en">Mixed cryoglobulinemia type II</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12397">
                                            <OrphaCode>93555</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93555</ExpertLink>
                                            <Name lang="en">Mixed cryoglobulinemia type III</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="17099">
                                        <OrphaCode>156152</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=156152</ExpertLink>
                                        <Name lang="en">Anti-neutrophil cytoplasmic antibody-associated vasculitis</Name>
                                        <DisorderType id="21436">
                                          <Name lang="en">Clinical group</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="3">
                                        <ClassificationNode>
                                          <Disorder id="745">
                                            <OrphaCode>183</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=183</ExpertLink>
                                            <Name lang="en">Eosinophilic granulomatosis with polyangiitis</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="753">
                                            <OrphaCode>727</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=727</ExpertLink>
                                            <Name lang="en">Microscopic polyangiitis</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="759">
                                            <OrphaCode>900</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=900</ExpertLink>
                                            <Name lang="en">Granulomatosis with polyangiitis</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20133">
                                <OrphaCode>264984</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264984</ExpertLink>
                                <Name lang="en">Exposure-related interstitial lung disease</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="9794">
                                    <OrphaCode>31740</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=31740</ExpertLink>
                                    <Name lang="en">Hypersensitivity pneumonitis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="32172">
                                        <OrphaCode>686462</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=686462</ExpertLink>
                                        <Name lang="en">Non-fibrotic hypersensitivity pneumonitis</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32173">
                                        <OrphaCode>686465</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=686465</ExpertLink>
                                        <Name lang="en">Fibrotic hypersensitivity pneumonitis</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20132">
                                    <OrphaCode>264978</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=264978</ExpertLink>
                                    <Name lang="en">Drug or radiation exposure-related interstitial lung disease</Name>
                                    <DisorderType id="21429">
                                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23102">
                                <OrphaCode>420259</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=420259</ExpertLink>
                                <Name lang="en">Secondary pulmonary alveolar proteinosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14505">
                                <OrphaCode>99932</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99932</ExpertLink>
                                <Name lang="en">Heiner syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="19132">
                    <OrphaCode>228426</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=228426</ExpertLink>
                    <Name lang="en">Syndromic multisystem autoimmune disease due to Itch deficiency</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="19523">
                    <OrphaCode>247522</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247522</ExpertLink>
                    <Name lang="en">Primary ciliary dyskinesia-retinitis pigmentosa syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23030">
                    <OrphaCode>411703</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=411703</ExpertLink>
                    <Name lang="en">Pulmonary non-tuberculous mycobacterial infection</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23394">
                    <OrphaCode>439881</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=439881</ExpertLink>
                    <Name lang="en">Plastic bronchitis</Name>
                    <DisorderType id="21429">
                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23209">
                    <OrphaCode>425120</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=425120</ExpertLink>
                    <Name lang="en">STING-associated vasculopathy with onset in infancy</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="21958">
                    <OrphaCode>330012</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=330012</ExpertLink>
                    <Name lang="en">High altitude pulmonary edema</Name>
                    <DisorderType id="21429">
                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="20900">
                    <OrphaCode>293987</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=293987</ExpertLink>
                    <Name lang="en">Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="26330">
                    <OrphaCode>505248</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=505248</ExpertLink>
                    <Name lang="en">Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="11957">
                    <OrphaCode>90066</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90066</ExpertLink>
                    <Name lang="en">Pneumonia caused by Pseudomonas aeruginosa infection</Name>
                    <DisorderType id="21429">
                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="28838">
                    <OrphaCode>576074</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=576074</ExpertLink>
                    <Name lang="en">Middle East respiratory syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23612">
                    <OrphaCode>449266</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=449266</ExpertLink>
                    <Name lang="en">Pleural empyema</Name>
                    <DisorderType id="21429">
                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23665">
                    <OrphaCode>454836</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=454836</ExpertLink>
                    <Name lang="en">Avian influenza</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="26354">
                    <OrphaCode>505395</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=505395</ExpertLink>
                    <Name lang="en">Ventilator-induced diaphragmatic dysfunction</Name>
                    <DisorderType id="21429">
                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="14376">
                    <OrphaCode>99803</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99803</ExpertLink>
                    <Name lang="en">Haddad syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="2497">
                    <OrphaCode>661</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=661</ExpertLink>
                    <Name lang="en">Congenital central hypoventilation syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18823">
                    <OrphaCode>217080</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217080</ExpertLink>
                    <Name lang="en">Pulmonary fungal infections in patients deemed at risk</Name>
                    <DisorderType id="21429">
                      <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="14554">
                    <OrphaCode>99981</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99981</ExpertLink>
                    <Name lang="en">Apnea of prematurity</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="32238">
                    <OrphaCode>692812</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=692812</ExpertLink>
                    <Name lang="en">RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="32167">
                    <OrphaCode>685082</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=685082</ExpertLink>
                    <Name lang="en">Pediatric acute respiratory distress syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="31793">
                    <OrphaCode>645814</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=645814</ExpertLink>
                    <Name lang="en">Primary pulmonary tuberculosis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="20721">
                    <OrphaCode>289390</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289390</ExpertLink>
                    <Name lang="en">Primary Sjögren disease</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
              </ClassificationNodeChildList>
            </ClassificationNode>
          </ClassificationNodeChildList>
        </ClassificationNode>
      </ClassificationNodeRootList>
    </Classification>
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</JDBOR>
