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                              <Disorder id="13866">
                                <OrphaCode>98849</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98849</ExpertLink>
                                <Name lang="en">Systemic mastocytosis with associated hematologic neoplasm</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13867">
                                <OrphaCode>98850</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98850</ExpertLink>
                                <Name lang="en">Aggressive systemic mastocytosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13868">
                                <OrphaCode>98851</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98851</ExpertLink>
                                <Name lang="en">Mast cell leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="28495">
                                    <OrphaCode>566393</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=566393</ExpertLink>
                                    <Name lang="en">Acute mast cell leukemia</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="28496">
                                    <OrphaCode>566396</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=566396</ExpertLink>
                                    <Name lang="en">Chronic mast cell leukemia</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17241">
                                <OrphaCode>158775</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=158775</ExpertLink>
                                <Name lang="en">Smoldering systemic mastocytosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17242">
                                <OrphaCode>158778</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=158778</ExpertLink>
                                <Name lang="en">Isolated bone marrow mastocytosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10894">
                            <OrphaCode>66646</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=66646</ExpertLink>
                            <Name lang="en">Cutaneous mastocytosis</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="11481">
                                <OrphaCode>79455</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79455</ExpertLink>
                                <Name lang="en">Cutaneous mastocytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11482">
                                <OrphaCode>79456</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79456</ExpertLink>
                                <Name lang="en">Diffuse cutaneous mastocytosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="20501">
                                    <OrphaCode>280785</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280785</ExpertLink>
                                    <Name lang="en">Bullous diffuse cutaneous mastocytosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20502">
                                    <OrphaCode>280794</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280794</ExpertLink>
                                    <Name lang="en">Pseudoxanthomatous diffuse cutaneous mastocytosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11483">
                                <OrphaCode>79457</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79457</ExpertLink>
                                <Name lang="en">Maculopapular cutaneous mastocytosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="4">
                                <ClassificationNode>
                                  <Disorder id="12033">
                                    <OrphaCode>90389</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90389</ExpertLink>
                                    <Name lang="en">Telangiectasia macularis eruptiva perstans</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="17238">
                                    <OrphaCode>158766</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=158766</ExpertLink>
                                    <Name lang="en">Typical urticaria pigmentosa</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="17239">
                                    <OrphaCode>158769</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=158769</ExpertLink>
                                    <Name lang="en">Plaque-form urticaria pigmentosa</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="17240">
                                    <OrphaCode>158772</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=158772</ExpertLink>
                                    <Name lang="en">Nodular urticaria pigmentosa</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10895">
                            <OrphaCode>66661</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=66661</ExpertLink>
                            <Name lang="en">Mast cell sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10896">
                            <OrphaCode>66662</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=66662</ExpertLink>
                            <Name lang="en">Extracutaneous mastocytoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17952">
                        <OrphaCode>171895</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171895</ExpertLink>
                        <Name lang="en">Myeloid hemopathy</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="3586">
                            <OrphaCode>519</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=519</ExpertLink>
                            <Name lang="en">Acute myeloid leukemia</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="6">
                            <ClassificationNode>
                              <Disorder id="11752">
                                <OrphaCode>86845</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86845</ExpertLink>
                                <Name lang="en">Acute myeloid leukaemia with myelodysplasia-related features</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11753">
                                <OrphaCode>86846</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86846</ExpertLink>
                                <Name lang="en">Therapy related acute myeloid leukemia and myelodysplastic syndrome</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="14978">
                                    <OrphaCode>102379</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=102379</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14979">
                                    <OrphaCode>102381</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=102381</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="17567">
                                    <OrphaCode>164726</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=164726</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia and myelodysplastic syndromes related to radiation</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11756">
                                <OrphaCode>86851</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86851</ExpertLink>
                                <Name lang="en">Acute leukemia of ambiguous lineage</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="13852">
                                    <OrphaCode>98835</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98835</ExpertLink>
                                    <Name lang="en">Acute undifferentiated leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="27686">
                                    <OrphaCode>530995</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=530995</ExpertLink>
                                    <Name lang="en">Mixed phenotype acute leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="29433">
                                        <OrphaCode>589534</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=589534</ExpertLink>
                                        <Name lang="en">Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)</Name>
                                        <DisorderType id="21443">
                                          <Name lang="en">Etiological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="29436">
                                        <OrphaCode>589595</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=589595</ExpertLink>
                                        <Name lang="en">Mixed phenotype acute leukemia with t(v;11q23.3)</Name>
                                        <DisorderType id="21443">
                                          <Name lang="en">Etiological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13294">
                                <OrphaCode>98277</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98277</ExpertLink>
                                <Name lang="en">Acute myeloid leukemia with recurrent genetic anomaly</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="12">
                                <ClassificationNode>
                                  <Disorder id="8559">
                                    <OrphaCode>520</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=520</ExpertLink>
                                    <Name lang="en">Acute promyelocytic leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="13846">
                                    <OrphaCode>98829</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98829</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="13848">
                                    <OrphaCode>98831</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98831</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with 11q23 abnormalities</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14981">
                                    <OrphaCode>102724</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=102724</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with t(8;21)(q22;q22) translocation</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21660">
                                    <OrphaCode>319480</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319480</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with CEBPA somatic mutations</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22467">
                                    <OrphaCode>370026</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370026</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with t(8;16)(p11;p13) translocation</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22869">
                                    <OrphaCode>402014</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=402014</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with t(6;9)(p23;q34)</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22870">
                                    <OrphaCode>402017</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=402017</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with t(9;11)(p22;q23)</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22871">
                                    <OrphaCode>402020</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=402020</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22872">
                                    <OrphaCode>402023</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=402023</ExpertLink>
                                    <Name lang="en">Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22873">
                                    <OrphaCode>402026</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=402026</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with NPM1 somatic mutations</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="29204">
                                    <OrphaCode>585867</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585867</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with t(9;22)(q34.1;q11.2)</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17684">
                                <OrphaCode>167714</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=167714</ExpertLink>
                                <Name lang="en">Unclassified acute myeloid leukemia</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="10">
                                <ClassificationNode>
                                  <Disorder id="8560">
                                    <OrphaCode>517</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=517</ExpertLink>
                                    <Name lang="en">Acute myelomonocytic leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="8561">
                                    <OrphaCode>514</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=514</ExpertLink>
                                    <Name lang="en">Acute monoblastic/monocytic leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="8562">
                                    <OrphaCode>318</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=318</ExpertLink>
                                    <Name lang="en">Acute erythroid leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="8563">
                                    <OrphaCode>518</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=518</ExpertLink>
                                    <Name lang="en">Acute megakaryoblastic leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="3">
                                    <ClassificationNode>
                                      <Disorder id="14460">
                                        <OrphaCode>99887</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99887</ExpertLink>
                                        <Name lang="en">Acute megakaryoblastic leukemia in children with Down syndrome</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="21935">
                                        <OrphaCode>329469</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=329469</ExpertLink>
                                        <Name lang="en">Acute megakaryoblastic leukemia in children without Down syndrome</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32019">
                                        <OrphaCode>662934</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662934</ExpertLink>
                                        <Name lang="en">Acute megakaryoblastic leukemia in adult</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11751">
                                    <OrphaCode>86843</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86843</ExpertLink>
                                    <Name lang="en">Acute panmyelosis with myelofibrosis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11754">
                                    <OrphaCode>86849</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86849</ExpertLink>
                                    <Name lang="en">Acute basophilic leukemia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11755">
                                    <OrphaCode>86850</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86850</ExpertLink>
                                    <Name lang="en">Myeloid sarcoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="13849">
                                    <OrphaCode>98832</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98832</ExpertLink>
                                    <Name lang="en">Acute myeloid leukemia with minimal differentiation</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="13850">
                                    <OrphaCode>98833</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98833</ExpertLink>
                                    <Name lang="en">Acute myeloblastic leukemia without maturation</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="13851">
                                    <OrphaCode>98834</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98834</ExpertLink>
                                    <Name lang="en">Acute myeloblastic leukemia with maturation</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21659">
                                <OrphaCode>319465</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319465</ExpertLink>
                                <Name lang="en">Inherited acute myeloid leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10703">
                            <OrphaCode>52688</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=52688</ExpertLink>
                            <Name lang="en">Myelodysplastic syndrome</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="6">
                            <ClassificationNode>
                              <Disorder id="11088">
                                <OrphaCode>75564</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=75564</ExpertLink>
                                <Name lang="en">Acquired idiopathic sideroblastic anemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11748">
                                <OrphaCode>86836</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86836</ExpertLink>
                                <Name lang="en">Refractory cytopenia with multilineage dysplasia</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="13843">
                                    <OrphaCode>98826</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98826</ExpertLink>
                                    <Name lang="en">Myelodysplastic neoplasm with low blasts</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="13844">
                                    <OrphaCode>98827</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98827</ExpertLink>
                                    <Name lang="en">Unclassified myelodysplastic syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="26578">
                                    <OrphaCode>508542</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=508542</ExpertLink>
                                    <Name lang="en">Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11749">
                                <OrphaCode>86839</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86839</ExpertLink>
                                <Name lang="en">Myelodysplastic neoplasm with increased blasts</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14592">
                                    <OrphaCode>100019</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100019</ExpertLink>
                                    <Name lang="en">Myelodysplastic neoplasm with increased blasts type 1</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14593">
                                    <OrphaCode>100020</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100020</ExpertLink>
                                    <Name lang="en">Myelodysplastic neoplasm with increased blasts type 2</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11750">
                                <OrphaCode>86841</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86841</ExpertLink>
                                <Name lang="en">Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17806">
                                <OrphaCode>168960</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168960</ExpertLink>
                                <Name lang="en">Refractory anemia with excess blasts in transformation</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="25813">
                                <OrphaCode>495930</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=495930</ExpertLink>
                                <Name lang="en">Familial monosomy 7 syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13291">
                            <OrphaCode>98274</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98274</ExpertLink>
                            <Name lang="en">Myeloproliferative neoplasm</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="12">
                            <ClassificationNode>
                              <Disorder id="3599">
                                <OrphaCode>3318</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3318</ExpertLink>
                                <Name lang="en">Essential thrombocythemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3705">
                                <OrphaCode>521</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=521</ExpertLink>
                                <Name lang="en">Chronic myeloid leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8745">
                                <OrphaCode>824</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=824</ExpertLink>
                                <Name lang="en">Primary myelofibrosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8747">
                                <OrphaCode>729</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=729</ExpertLink>
                                <Name lang="en">Polycythemia vera</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11744">
                                <OrphaCode>86829</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86829</ExpertLink>
                                <Name lang="en">Chronic neutrophilic leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11745">
                                <OrphaCode>86830</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86830</ExpertLink>
                                <Name lang="en">Chronic myeloproliferative disease, unclassifiable</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17800">
                                <OrphaCode>168940</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168940</ExpertLink>
                                <Name lang="en">Chronic eosinophilic leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17805">
                                <OrphaCode>168956</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168956</ExpertLink>
                                <Name lang="en">Hypereosinophilic syndrome</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="3422">
                                    <OrphaCode>3260</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3260</ExpertLink>
                                    <Name lang="en">Idiopathic hypereosinophilic syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21543">
                                    <OrphaCode>314950</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314950</ExpertLink>
                                    <Name lang="en">Primary hypereosinophilic syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21544">
                                    <OrphaCode>314962</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314962</ExpertLink>
                                    <Name lang="en">Secondary hypereosinophilic syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="1">
                                    <ClassificationNode>
                                      <Disorder id="21545">
                                        <OrphaCode>314970</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314970</ExpertLink>
                                        <Name lang="en">Lymphocytic hypereosinophilic syndrome</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23117">
                                <OrphaCode>420611</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=420611</ExpertLink>
                                <Name lang="en">Transient myeloproliferative syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="25223">
                                <OrphaCode>480851</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=480851</ExpertLink>
                                <Name lang="en">Hereditary thrombocytopenia with early-onset myelofibrosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="25397">
                                <OrphaCode>488280</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=488280</ExpertLink>
                                <Name lang="en">14q32 duplication syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32128">
                                <OrphaCode>675775</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675775</ExpertLink>
                                <Name lang="en">Severe congenital myelofibrosis-pancytopenia-intellectual disability-neurologic and ophthalmic abnormalities syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13292">
                            <OrphaCode>98275</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98275</ExpertLink>
                            <Name lang="en">Myelodysplastic/myeloproliferative disease</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="11747">
                                <OrphaCode>86834</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86834</ExpertLink>
                                <Name lang="en">Juvenile myelomonocytic leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13840">
                                <OrphaCode>98823</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98823</ExpertLink>
                                <Name lang="en">Chronic myelomonocytic leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13841">
                                <OrphaCode>98824</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98824</ExpertLink>
                                <Name lang="en">Atypical chronic myeloid leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13842">
                                <OrphaCode>98825</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98825</ExpertLink>
                                <Name lang="en">Unclassified myelodysplastic/myeloproliferative disease</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17801">
                            <OrphaCode>168943</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168943</ExpertLink>
                            <Name lang="en">Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="17802">
                                <OrphaCode>168947</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168947</ExpertLink>
                                <Name lang="en">Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17803">
                                <OrphaCode>168950</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168950</ExpertLink>
                                <Name lang="en">Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17804">
                                <OrphaCode>168953</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168953</ExpertLink>
                                <Name lang="en">Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="29434">
                                <OrphaCode>589542</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=589542</ExpertLink>
                                <Name lang="en">Myeloid/lymphoid neoplasm associated with JAK2 rearrangement</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17953">
                        <OrphaCode>171898</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171898</ExpertLink>
                        <Name lang="en">Lymphoid hemopathy</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="8">
                        <ClassificationNode>
                          <Disorder id="3468">
                            <OrphaCode>3261</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3261</ExpertLink>
                            <Name lang="en">Autoimmune lymphoproliferative syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3618">
                            <OrphaCode>160</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=160</ExpertLink>
                            <Name lang="en">Castleman disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="12466">
                                <OrphaCode>93685</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93685</ExpertLink>
                                <Name lang="en">Unicentric Castleman disease</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28674">
                                <OrphaCode>570431</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=570431</ExpertLink>
                                <Name lang="en">Idiopathic multicentric Castleman disease</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28675">
                                <OrphaCode>570438</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=570438</ExpertLink>
                                <Name lang="en">HHV-8-associated multicentric Castleman disease</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13299">
                            <OrphaCode>98282</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98282</ExpertLink>
                            <Name lang="en">Plasma cell tumor</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="7">
                            <ClassificationNode>
                              <Disorder id="2627">
                                <OrphaCode>2905</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2905</ExpertLink>
                                <Name lang="en">POEMS syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8776">
                                <OrphaCode>29073</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=29073</ExpertLink>
                                <Name lang="en">Multiple myeloma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11717">
                                <OrphaCode>85443</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85443</ExpertLink>
                                <Name lang="en">AL amyloidosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="21517">
                                    <OrphaCode>314701</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314701</ExpertLink>
                                    <Name lang="en">Primary systemic amyloidosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21518">
                                    <OrphaCode>314709</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314709</ExpertLink>
                                    <Name lang="en">Primary localized amyloidosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11759">
                                <OrphaCode>86855</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86855</ExpertLink>
                                <Name lang="en">Plasmacytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14594">
                                    <OrphaCode>100021</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100021</ExpertLink>
                                    <Name lang="en">Primary plasmacytoma of the bone</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14595">
                                    <OrphaCode>100022</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100022</ExpertLink>
                                    <Name lang="en">Extramedullary soft tissue plasmacytoma</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11760">
                                <OrphaCode>86861</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86861</ExpertLink>
                                <Name lang="en">Non-amyloid monoclonal immunoglobulin deposition disease</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="12398">
                                    <OrphaCode>93556</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93556</ExpertLink>
                                    <Name lang="en">Heavy chain deposition disease</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12399">
                                    <OrphaCode>93557</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93557</ExpertLink>
                                    <Name lang="en">Light and heavy chain deposition disease</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12400">
                                    <OrphaCode>93558</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93558</ExpertLink>
                                    <Name lang="en">Light chain deposition disease</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11761">
                                <OrphaCode>86864</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86864</ExpertLink>
                                <Name lang="en">Heavy chain disease</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="14597">
                                    <OrphaCode>100024</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100024</ExpertLink>
                                    <Name lang="en">Mu-heavy chain disease</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14598">
                                    <OrphaCode>100025</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100025</ExpertLink>
                                    <Name lang="en">Alpha-heavy chain disease</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14599">
                                    <OrphaCode>100026</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100026</ExpertLink>
                                    <Name lang="en">Gamma-heavy chain disease</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23656">
                                <OrphaCode>454714</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=454714</ExpertLink>
                                <Name lang="en">Plasma cell leukemia</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13304">
                            <OrphaCode>98287</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98287</ExpertLink>
                            <Name lang="en">Histiocytic and dendritic cell tumor</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="13305">
                                <OrphaCode>98288</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98288</ExpertLink>
                                <Name lang="en">Macrophage or histiocytic tumor</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="1">
                                <ClassificationNode>
                                  <Disorder id="11776">
                                    <OrphaCode>86896</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86896</ExpertLink>
                                    <Name lang="en">Histiocytic sarcoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13306">
                                <OrphaCode>98289</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98289</ExpertLink>
                                <Name lang="en">Dendritic cell tumor</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <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="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>
                                    <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="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="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>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11777">
                                    <OrphaCode>86897</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86897</ExpertLink>
                                    <Name lang="en">Langerhans cell sarcoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11778">
                                    <OrphaCode>86900</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86900</ExpertLink>
                                    <Name lang="en">Interdigitating dendritic cell sarcoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11780">
                                    <OrphaCode>86903</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86903</ExpertLink>
                                    <Name lang="en">Dendritic cell sarcoma not otherwise specified</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="17177">
                                    <OrphaCode>158019</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=158019</ExpertLink>
                                    <Name lang="en">Indeterminate cell histiocytosis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13307">
                            <OrphaCode>98290</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98290</ExpertLink>
                            <Name lang="en">Immunodeficiency-associated lymphoproliferative disease</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="10952">
                                <OrphaCode>70568</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70568</ExpertLink>
                                <Name lang="en">Post-transplant lymphoproliferative disease</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11781">
                                <OrphaCode>86904</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86904</ExpertLink>
                                <Name lang="en">Methotrexate-associated lymphoproliferative disorders</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13308">
                                <OrphaCode>98291</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98291</ExpertLink>
                                <Name lang="en">Lymphoproliferative disease associated with primary immune disease</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32119">
                                <OrphaCode>675628</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675628</ExpertLink>
                                <Name lang="en">TLR8-related inflammation-severe neutropenia-bone marrow failure-lymphoproliferation syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18975">
                            <OrphaCode>223735</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=223735</ExpertLink>
                            <Name lang="en">Lymphoma</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="3765">
                                <OrphaCode>547</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=547</ExpertLink>
                                <Name lang="en">Non-Hodgkin lymphoma</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="3732">
                                    <OrphaCode>513</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=513</ExpertLink>
                                    <Name lang="en">Acute lymphoblastic leukemia</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="14433">
                                        <OrphaCode>99860</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99860</ExpertLink>
                                        <Name lang="en">Precursor B-cell acute lymphoblastic leukemia</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="9">
                                        <ClassificationNode>
                                          <Disorder id="29211">
                                            <OrphaCode>585909</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585909</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="29212">
                                            <OrphaCode>585918</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585918</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="29213">
                                            <OrphaCode>585929</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585929</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="29214">
                                            <OrphaCode>585936</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585936</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with hyperdiploidy</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="29215">
                                            <OrphaCode>585942</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585942</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with hypodiploidy</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="29216">
                                            <OrphaCode>585948</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585948</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="29217">
                                            <OrphaCode>585956</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=585956</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="31717">
                                            <OrphaCode>641372</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=641372</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="31718">
                                            <OrphaCode>641375</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=641375</ExpertLink>
                                            <Name lang="en">B-lymphoblastic leukemia/lymphoma with t(17;19)</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14434">
                                        <OrphaCode>99861</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99861</ExpertLink>
                                        <Name lang="en">Precursor T-cell acute lymphoblastic leukemia</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="17955">
                                    <OrphaCode>171915</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171915</ExpertLink>
                                    <Name lang="en">B-cell non-Hodgkin lymphoma</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="21143">
                                        <OrphaCode>300842</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300842</ExpertLink>
                                        <Name lang="en">Indolent B-cell non-Hodgkin lymphoma</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="8">
                                        <ClassificationNode>
                                          <Disorder id="8750">
                                            <OrphaCode>545</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=545</ExpertLink>
                                            <Name lang="en">Follicular lymphoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="10313">
                                            <OrphaCode>33226</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33226</ExpertLink>
                                            <Name lang="en">Waldenström macroglobulinemia</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="10778">
                                            <OrphaCode>58017</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=58017</ExpertLink>
                                            <Name lang="en">Classic hairy cell leukemia</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="10899">
                                            <OrphaCode>67038</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=67038</ExpertLink>
                                            <Name lang="en">B-cell chronic lymphocytic leukemia</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18051">
                                            <OrphaCode>178557</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178557</ExpertLink>
                                            <Name lang="en">Indolent primary cutaneous B-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="2">
                                            <ClassificationNode>
                                              <Disorder id="18045">
                                                <OrphaCode>178536</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178536</ExpertLink>
                                                <Name lang="en">Primary cutaneous marginal zone B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18046">
                                                <OrphaCode>178540</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178540</ExpertLink>
                                                <Name lang="en">Primary cutaneous follicle center lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="21149">
                                            <OrphaCode>300878</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300878</ExpertLink>
                                            <Name lang="en">Hairy cell leukemia variant</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="21153">
                                            <OrphaCode>300912</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300912</ExpertLink>
                                            <Name lang="en">Marginal zone lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="4">
                                            <ClassificationNode>
                                              <Disorder id="10694">
                                                <OrphaCode>52417</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=52417</ExpertLink>
                                                <Name lang="en">MALT lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11758">
                                                <OrphaCode>86854</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86854</ExpertLink>
                                                <Name lang="en">Splenic marginal zone lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11762">
                                                <OrphaCode>86867</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86867</ExpertLink>
                                                <Name lang="en">Nodal marginal zone B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="21148">
                                                <OrphaCode>300869</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300869</ExpertLink>
                                                <Name lang="en">Splenic diffuse red pulp small B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="23445">
                                            <OrphaCode>443159</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=443159</ExpertLink>
                                            <Name lang="en">Lymphoplasmacytic lymphoma without IgM production</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="21144">
                                        <OrphaCode>300846</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300846</ExpertLink>
                                        <Name lang="en">Aggressive B-cell non-Hodgkin lymphoma</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="8">
                                        <ClassificationNode>
                                          <Disorder id="3747">
                                            <OrphaCode>543</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=543</ExpertLink>
                                            <Name lang="en">Burkitt lymphoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="8749">
                                            <OrphaCode>544</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=544</ExpertLink>
                                            <Name lang="en">Diffuse large B-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="9">
                                            <ClassificationNode>
                                              <Disorder id="11763">
                                                <OrphaCode>86869</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86869</ExpertLink>
                                                <Name lang="en">Lymphomatoid granulomatosis</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="13855">
                                                <OrphaCode>98838</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98838</ExpertLink>
                                                <Name lang="en">Primary mediastinal large B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="13856">
                                                <OrphaCode>98839</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98839</ExpertLink>
                                                <Name lang="en">Intravascular large B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="20756">
                                                <OrphaCode>289661</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289661</ExpertLink>
                                                <Name lang="en">Epstein-Barr virus-positive diffuse large B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="21145">
                                                <OrphaCode>300849</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300849</ExpertLink>
                                                <Name lang="en">Diffuse large B-cell lymphoma of the central nervous system</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="21146">
                                                <OrphaCode>300857</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300857</ExpertLink>
                                                <Name lang="en">T-cell/histiocyte rich large B cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="21150">
                                                <OrphaCode>300888</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300888</ExpertLink>
                                                <Name lang="en">Diffuse large B-cell lymphoma with chronic inflammation</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="22363">
                                                <OrphaCode>364043</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=364043</ExpertLink>
                                                <Name lang="en">ALK-positive large B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="32302">
                                                <OrphaCode>695631</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=695631</ExpertLink>
                                                <Name lang="en">Primary vitreoretinal large B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="10631">
                                            <OrphaCode>48686</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=48686</ExpertLink>
                                            <Name lang="en">Primary effusion lymphoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="10693">
                                            <OrphaCode>52416</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=52416</ExpertLink>
                                            <Name lang="en">Mantle cell lymphoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="11757">
                                            <OrphaCode>86852</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86852</ExpertLink>
                                            <Name lang="en">B-cell prolymphocytic leukemia</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18050">
                                            <OrphaCode>178554</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178554</ExpertLink>
                                            <Name lang="en">Aggressive primary cutaneous B-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="1">
                                            <ClassificationNode>
                                              <Disorder id="18047">
                                                <OrphaCode>178544</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178544</ExpertLink>
                                                <Name lang="en">Primary cutaneous diffuse large B-cell lymphoma, leg type</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="20757">
                                            <OrphaCode>289666</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289666</ExpertLink>
                                            <Name lang="en">Plasmablastic lymphoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="25216">
                                            <OrphaCode>480541</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=480541</ExpertLink>
                                            <Name lang="en">High grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="17956">
                                    <OrphaCode>171918</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171918</ExpertLink>
                                    <Name lang="en">T-cell non-Hodgkin lymphoma</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="14">
                                    <ClassificationNode>
                                      <Disorder id="10952">
                                        <OrphaCode>70568</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70568</ExpertLink>
                                        <Name lang="en">Post-transplant lymphoproliferative disease</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11764">
                                        <OrphaCode>86870</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86870</ExpertLink>
                                        <Name lang="en">Blastic plasmacytoid dendritic cell neoplasm</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11765">
                                        <OrphaCode>86871</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86871</ExpertLink>
                                        <Name lang="en">T-cell prolymphocytic leukemia</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11770">
                                        <OrphaCode>86880</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86880</ExpertLink>
                                        <Name lang="en">Enteropathy-associated T-cell lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11771">
                                        <OrphaCode>86882</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86882</ExpertLink>
                                        <Name lang="en">Hepatosplenic T-cell lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11774">
                                        <OrphaCode>86886</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86886</ExpertLink>
                                        <Name lang="en">Angioimmunoblastic T-cell lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="13858">
                                        <OrphaCode>98841</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98841</ExpertLink>
                                        <Name lang="en">Anaplastic large cell lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="21151">
                                            <OrphaCode>300895</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300895</ExpertLink>
                                            <Name lang="en">ALK-positive anaplastic large cell lymphoma</Name>
                                            <DisorderType id="21457">
                                              <Name lang="en">Histopathological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="21152">
                                            <OrphaCode>300903</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300903</ExpertLink>
                                            <Name lang="en">ALK-negative anaplastic large cell lymphoma</Name>
                                            <DisorderType id="21457">
                                              <Name lang="en">Histopathological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="17954">
                                        <OrphaCode>171901</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171901</ExpertLink>
                                        <Name lang="en">Primary cutaneous T-cell lymphoma</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="18048">
                                            <OrphaCode>178548</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178548</ExpertLink>
                                            <Name lang="en">Indolent primary cutaneous T-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="4">
                                            <ClassificationNode>
                                              <Disorder id="3749">
                                                <OrphaCode>541</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=541</ExpertLink>
                                                <Name lang="en">Primary cutaneous CD30+ T-cell lymphoproliferative disease</Name>
                                                <DisorderType id="21436">
                                                  <Name lang="en">Clinical group</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="2">
                                                <ClassificationNode>
                                                  <Disorder id="13859">
                                                    <OrphaCode>98842</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98842</ExpertLink>
                                                    <Name lang="en">Lymphomatoid papulosis</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="21147">
                                                    <OrphaCode>300865</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300865</ExpertLink>
                                                    <Name lang="en">Primary cutaneous anaplastic large cell lymphoma</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11772">
                                                <OrphaCode>86884</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86884</ExpertLink>
                                                <Name lang="en">Subcutaneous panniculitis-like T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18040">
                                                <OrphaCode>178522</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178522</ExpertLink>
                                                <Name lang="en">Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18054">
                                                <OrphaCode>178566</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178566</ExpertLink>
                                                <Name lang="en">Mycosis fungoides and variants</Name>
                                                <DisorderType id="21436">
                                                  <Name lang="en">Clinical group</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="4">
                                                <ClassificationNode>
                                                  <Disorder id="3400">
                                                    <OrphaCode>2584</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2584</ExpertLink>
                                                    <Name lang="en">Classic mycosis fungoides</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="10311">
                                                    <OrphaCode>33111</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33111</ExpertLink>
                                                    <Name lang="en">Granulomatous slack skin</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="18038">
                                                    <OrphaCode>178512</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178512</ExpertLink>
                                                    <Name lang="en">Folliculotropic mycosis fungoides</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="18039">
                                                    <OrphaCode>178517</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178517</ExpertLink>
                                                    <Name lang="en">Localized pagetoid reticulosis</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18049">
                                            <OrphaCode>178551</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178551</ExpertLink>
                                            <Name lang="en">Aggressive primary cutaneous T-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="6">
                                            <ClassificationNode>
                                              <Disorder id="3401">
                                                <OrphaCode>3162</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3162</ExpertLink>
                                                <Name lang="en">Sézary syndrome</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11768">
                                                <OrphaCode>86875</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86875</ExpertLink>
                                                <Name lang="en">Adult T-cell leukemia/lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11769">
                                                <OrphaCode>86879</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86879</ExpertLink>
                                                <Name lang="en">Extranodal nasal NK/T cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11773">
                                                <OrphaCode>86885</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86885</ExpertLink>
                                                <Name lang="en">Primary cutaneous peripheral T-cell lymphoma not otherwise specified</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18042">
                                                <OrphaCode>178528</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178528</ExpertLink>
                                                <Name lang="en">Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18044">
                                                <OrphaCode>178533</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178533</ExpertLink>
                                                <Name lang="en">Primary cutaneous gamma/delta-positive T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="22361">
                                        <OrphaCode>364033</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=364033</ExpertLink>
                                        <Name lang="en">Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="22362">
                                        <OrphaCode>364039</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=364039</ExpertLink>
                                        <Name lang="en">Hydroa vacciniforme-like lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="26906">
                                        <OrphaCode>512034</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=512034</ExpertLink>
                                        <Name lang="en">Large granular lymphocyte leukemia</Name>
                                        <DisorderType id="21436">
                                          <Name lang="en">Clinical group</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="3">
                                        <ClassificationNode>
                                          <Disorder id="11766">
                                            <OrphaCode>86872</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86872</ExpertLink>
                                            <Name lang="en">T-cell large granular lymphocyte leukemia</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="11767">
                                            <OrphaCode>86873</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86873</ExpertLink>
                                            <Name lang="en">Aggressive NK-cell leukemia</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="26905">
                                            <OrphaCode>512017</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=512017</ExpertLink>
                                            <Name lang="en">Chronic lymphoproliferative disorder of natural killer cells</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="31899">
                                        <OrphaCode>652650</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652650</ExpertLink>
                                        <Name lang="en">Nodal T-follicular helper cell lymphoma, follicular type</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="31900">
                                        <OrphaCode>652658</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652658</ExpertLink>
                                        <Name lang="en">Monomorphic epitheliotropic intestinal T-cell lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32072">
                                        <OrphaCode>667662</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=667662</ExpertLink>
                                        <Name lang="en">Breast implant-associated anaplastic large cell lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13310">
                                <OrphaCode>98293</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98293</ExpertLink>
                                <Name lang="en">Hodgkin lymphoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="3739">
                                    <OrphaCode>391</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=391</ExpertLink>
                                    <Name lang="en">Classic Hodgkin lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="4">
                                    <ClassificationNode>
                                      <Disorder id="13860">
                                        <OrphaCode>98843</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98843</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, nodular sclerosis type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="13861">
                                        <OrphaCode>98844</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98844</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, mixed cellularity type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="13862">
                                        <OrphaCode>98845</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98845</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, lymphocyte-rich type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="13863">
                                        <OrphaCode>98846</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98846</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, lymphocyte-depleted type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11775">
                                    <OrphaCode>86893</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86893</ExpertLink>
                                    <Name lang="en">Nodular lymphocyte predominant Hodgkin lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17807">
                                <OrphaCode>168966</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168966</ExpertLink>
                                <Name lang="en">Composite lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20413">
                                <OrphaCode>279911</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=279911</ExpertLink>
                                <Name lang="en">Primary organ-specific lymphoma</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="8">
                                <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="3340">
                                    <OrphaCode>542</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=542</ExpertLink>
                                    <Name lang="en">Primary cutaneous lymphoma</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="17954">
                                        <OrphaCode>171901</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171901</ExpertLink>
                                        <Name lang="en">Primary cutaneous T-cell lymphoma</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="18048">
                                            <OrphaCode>178548</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178548</ExpertLink>
                                            <Name lang="en">Indolent primary cutaneous T-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="4">
                                            <ClassificationNode>
                                              <Disorder id="3749">
                                                <OrphaCode>541</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=541</ExpertLink>
                                                <Name lang="en">Primary cutaneous CD30+ T-cell lymphoproliferative disease</Name>
                                                <DisorderType id="21436">
                                                  <Name lang="en">Clinical group</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="2">
                                                <ClassificationNode>
                                                  <Disorder id="13859">
                                                    <OrphaCode>98842</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98842</ExpertLink>
                                                    <Name lang="en">Lymphomatoid papulosis</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="21147">
                                                    <OrphaCode>300865</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300865</ExpertLink>
                                                    <Name lang="en">Primary cutaneous anaplastic large cell lymphoma</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11772">
                                                <OrphaCode>86884</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86884</ExpertLink>
                                                <Name lang="en">Subcutaneous panniculitis-like T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18040">
                                                <OrphaCode>178522</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178522</ExpertLink>
                                                <Name lang="en">Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18054">
                                                <OrphaCode>178566</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178566</ExpertLink>
                                                <Name lang="en">Mycosis fungoides and variants</Name>
                                                <DisorderType id="21436">
                                                  <Name lang="en">Clinical group</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="4">
                                                <ClassificationNode>
                                                  <Disorder id="3400">
                                                    <OrphaCode>2584</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2584</ExpertLink>
                                                    <Name lang="en">Classic mycosis fungoides</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="10311">
                                                    <OrphaCode>33111</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33111</ExpertLink>
                                                    <Name lang="en">Granulomatous slack skin</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="18038">
                                                    <OrphaCode>178512</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178512</ExpertLink>
                                                    <Name lang="en">Folliculotropic mycosis fungoides</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                                <ClassificationNode>
                                                  <Disorder id="18039">
                                                    <OrphaCode>178517</OrphaCode>
                                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178517</ExpertLink>
                                                    <Name lang="en">Localized pagetoid reticulosis</Name>
                                                    <DisorderType id="21394">
                                                      <Name lang="en">Disease</Name>
                                                    </DisorderType>
                                                  </Disorder>
                                                  <ClassificationNodeChildList count="0">
                                                  </ClassificationNodeChildList>
                                                </ClassificationNode>
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18049">
                                            <OrphaCode>178551</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178551</ExpertLink>
                                            <Name lang="en">Aggressive primary cutaneous T-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="6">
                                            <ClassificationNode>
                                              <Disorder id="3401">
                                                <OrphaCode>3162</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3162</ExpertLink>
                                                <Name lang="en">Sézary syndrome</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11768">
                                                <OrphaCode>86875</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86875</ExpertLink>
                                                <Name lang="en">Adult T-cell leukemia/lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11769">
                                                <OrphaCode>86879</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86879</ExpertLink>
                                                <Name lang="en">Extranodal nasal NK/T cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="11773">
                                                <OrphaCode>86885</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86885</ExpertLink>
                                                <Name lang="en">Primary cutaneous peripheral T-cell lymphoma not otherwise specified</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18042">
                                                <OrphaCode>178528</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178528</ExpertLink>
                                                <Name lang="en">Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18044">
                                                <OrphaCode>178533</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178533</ExpertLink>
                                                <Name lang="en">Primary cutaneous gamma/delta-positive T-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="18053">
                                        <OrphaCode>178563</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178563</ExpertLink>
                                        <Name lang="en">Primary cutaneous B-cell lymphoma</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="18050">
                                            <OrphaCode>178554</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178554</ExpertLink>
                                            <Name lang="en">Aggressive primary cutaneous B-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="1">
                                            <ClassificationNode>
                                              <Disorder id="18047">
                                                <OrphaCode>178544</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178544</ExpertLink>
                                                <Name lang="en">Primary cutaneous diffuse large B-cell lymphoma, leg type</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18051">
                                            <OrphaCode>178557</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178557</ExpertLink>
                                            <Name lang="en">Indolent primary cutaneous B-cell lymphoma</Name>
                                            <DisorderType id="21436">
                                              <Name lang="en">Clinical group</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="2">
                                            <ClassificationNode>
                                              <Disorder id="18045">
                                                <OrphaCode>178536</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178536</ExpertLink>
                                                <Name lang="en">Primary cutaneous marginal zone B-cell lymphoma</Name>
                                                <DisorderType id="21394">
                                                  <Name lang="en">Disease</Name>
                                                </DisorderType>
                                              </Disorder>
                                              <ClassificationNodeChildList count="0">
                                              </ClassificationNodeChildList>
                                            </ClassificationNode>
                                            <ClassificationNode>
                                              <Disorder id="18046">
                                                <OrphaCode>178540</OrphaCode>
                                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178540</ExpertLink>
                                                <Name lang="en">Primary cutaneous follicle center lymphoma</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="10593">
                                    <OrphaCode>46135</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=46135</ExpertLink>
                                    <Name lang="en">Primary central nervous system lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12879">
                                    <OrphaCode>97285</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97285</ExpertLink>
                                    <Name lang="en">Thyroid lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20411">
                                    <OrphaCode>279897</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=279897</ExpertLink>
                                    <Name lang="en">Primary oculocerebral lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21514">
                                    <OrphaCode>314684</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314684</ExpertLink>
                                    <Name lang="en">Primary bone lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21689">
                                    <OrphaCode>319667</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319667</ExpertLink>
                                    <Name lang="en">Primary lymphoma of the conjunctiva</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32545">
                                    <OrphaCode>714046</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714046</ExpertLink>
                                    <Name lang="en">Primary choroidal lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20165">
                            <OrphaCode>268114</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=268114</ExpertLink>
                            <Name lang="en">RAS-associated autoimmune leukoproliferative disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21111">
                            <OrphaCode>300324</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300324</ExpertLink>
                            <Name lang="en">Persistent polyclonal B-cell lymphocytosis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="27593">
                        <OrphaCode>529468</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=529468</ExpertLink>
                        <Name lang="en">Monoclonal mast cell activation syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10552">
                    <OrphaCode>68411</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=68411</ExpertLink>
                    <Name lang="en">Rare bone tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="14">
                    <ClassificationNode>
                      <Disorder id="2257">
                        <OrphaCode>296</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=296</ExpertLink>
                        <Name lang="en">Ollier disease</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2515">
                        <OrphaCode>2760</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2760</ExpertLink>
                        <Name lang="en">OSLAM syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3247">
                        <OrphaCode>321</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=321</ExpertLink>
                        <Name lang="en">Multiple osteochondromas</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="6023">
                        <OrphaCode>178</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178</ExpertLink>
                        <Name lang="en">Chordoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10763">
                        <OrphaCode>55881</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=55881</ExpertLink>
                        <Name lang="en">Adamantinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10779">
                        <OrphaCode>58040</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=58040</ExpertLink>
                        <Name lang="en">Osteoblastoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="11578">
                        <OrphaCode>83468</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=83468</ExpertLink>
                        <Name lang="en">Solitary bone cyst</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="11645">
                        <OrphaCode>85182</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85182</ExpertLink>
                        <Name lang="en">Diaphyseal medullary stenosis-bone malignancy syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17509">
                        <OrphaCode>163634</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=163634</ExpertLink>
                        <Name lang="en">Maffucci syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18974">
                        <OrphaCode>223727</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=223727</ExpertLink>
                        <Name lang="en">Bone sarcoma</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="7">
                        <ClassificationNode>
                          <Disorder id="3530">
                            <OrphaCode>2023</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2023</ExpertLink>
                            <Name lang="en">Undifferentiated pleomorphic sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3734">
                            <OrphaCode>2030</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2030</ExpertLink>
                            <Name lang="en">Fibrosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3758">
                            <OrphaCode>668</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=668</ExpertLink>
                            <Name lang="en">Osteosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3759">
                            <OrphaCode>319</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319</ExpertLink>
                            <Name lang="en">Skeletal Ewing sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10762">
                            <OrphaCode>55880</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=55880</ExpertLink>
                            <Name lang="en">Chondrosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22354">
                            <OrphaCode>363976</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363976</ExpertLink>
                            <Name lang="en">Giant cell tumor of bone</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22491">
                            <OrphaCode>370348</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370348</ExpertLink>
                            <Name lang="en">Peripheral primitive neuroectodermal tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22932">
                        <OrphaCode>404507</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404507</ExpertLink>
                        <Name lang="en">Chondromyxoid fibroma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23291">
                        <OrphaCode>435329</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=435329</ExpertLink>
                        <Name lang="en">Familial ossifying fibroma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="25218">
                        <OrphaCode>480553</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=480553</ExpertLink>
                        <Name lang="en">Aneurysmal bone cyst</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32307">
                        <OrphaCode>696078</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=696078</ExpertLink>
                        <Name lang="en">Central giant cell granuloma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10985">
                    <OrphaCode>71209</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=71209</ExpertLink>
                    <Name lang="en">Rare soft tissue tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="15">
                    <ClassificationNode>
                      <Disorder id="1959">
                        <OrphaCode>2028</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2028</ExpertLink>
                        <Name lang="en">Juvenile hyaline fibromatosis</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3544">
                        <OrphaCode>2122</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2122</ExpertLink>
                        <Name lang="en">Kaposiform hemangioendothelioma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3545">
                        <OrphaCode>2591</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2591</ExpertLink>
                        <Name lang="en">Infantile myofibromatosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="4052">
                        <OrphaCode>3394</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3394</ExpertLink>
                        <Name lang="en">Soft tissue sarcoma</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="26">
                        <ClassificationNode>
                          <Disorder id="883">
                            <OrphaCode>780</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=780</ExpertLink>
                            <Name lang="en">Rhabdomyosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="14330">
                                <OrphaCode>99757</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99757</ExpertLink>
                                <Name lang="en">Embryonal rhabdomyosarcoma</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20843">
                                <OrphaCode>293199</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=293199</ExpertLink>
                                <Name lang="en">Pleomorphic rhabdomyosarcoma</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14329">
                                <OrphaCode>99756</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99756</ExpertLink>
                                <Name lang="en">Alveolar rhabdomyosarcoma</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3530">
                            <OrphaCode>2023</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2023</ExpertLink>
                            <Name lang="en">Undifferentiated pleomorphic sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3734">
                            <OrphaCode>2030</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2030</ExpertLink>
                            <Name lang="en">Fibrosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3735">
                            <OrphaCode>2126</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2126</ExpertLink>
                            <Name lang="en">Solitary fibrous tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3737">
                            <OrphaCode>3148</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3148</ExpertLink>
                            <Name lang="en">Malignant peripheral nerve sheath tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="19722">
                                <OrphaCode>252128</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252128</ExpertLink>
                                <Name lang="en">Malignant peripheral nerve sheath tumor with perineurial differentiation</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19733">
                                <OrphaCode>252212</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252212</ExpertLink>
                                <Name lang="en">Malignant triton tumor</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3738">
                            <OrphaCode>3273</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3273</ExpertLink>
                            <Name lang="en">Synovial sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="9285">
                            <OrphaCode>31112</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=31112</ExpertLink>
                            <Name lang="en">Dermatofibrosarcoma protuberans</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10316">
                            <OrphaCode>33276</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33276</ExpertLink>
                            <Name lang="en">Kaposi sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10838">
                            <OrphaCode>64720</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=64720</ExpertLink>
                            <Name lang="en">Leiomyosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10913">
                            <OrphaCode>69077</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=69077</ExpertLink>
                            <Name lang="en">Rhabdoid tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10914">
                            <OrphaCode>69078</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=69078</ExpertLink>
                            <Name lang="en">Liposarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="14540">
                                <OrphaCode>99967</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99967</ExpertLink>
                                <Name lang="en">Myxoid/round cell liposarcoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14542">
                                <OrphaCode>99969</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99969</ExpertLink>
                                <Name lang="en">Pleomorphic liposarcoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14543">
                                <OrphaCode>99970</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99970</ExpertLink>
                                <Name lang="en">Dedifferentiated liposarcoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14544">
                                <OrphaCode>99971</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99971</ExpertLink>
                                <Name lang="en">Well-differentiated liposarcoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11147">
                            <OrphaCode>79105</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79105</ExpertLink>
                            <Name lang="en">Myxofibrosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11579">
                            <OrphaCode>83469</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=83469</ExpertLink>
                            <Name lang="en">Desmoplastic small round cell tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11779">
                            <OrphaCode>86902</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86902</ExpertLink>
                            <Name lang="en">Follicular dendritic cell sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14539">
                            <OrphaCode>99966</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99966</ExpertLink>
                            <Name lang="en">Atypical teratoid rhabdoid tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17527">
                            <OrphaCode>163699</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=163699</ExpertLink>
                            <Name lang="en">Alveolar soft tissue sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18668">
                            <OrphaCode>209916</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=209916</ExpertLink>
                            <Name lang="en">Extraskeletal myxoid chondrosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20050">
                            <OrphaCode>263413</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263413</ExpertLink>
                            <Name lang="en">Angiosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20844">
                            <OrphaCode>293202</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=293202</ExpertLink>
                            <Name lang="en">Epithelioid sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22490">
                            <OrphaCode>370334</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370334</ExpertLink>
                            <Name lang="en">Extraskeletal Ewing sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22491">
                            <OrphaCode>370348</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370348</ExpertLink>
                            <Name lang="en">Peripheral primitive neuroectodermal tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <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="29460">
                            <OrphaCode>590539</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=590539</ExpertLink>
                            <Name lang="en">Isolated melanotic schwannoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="33057">
                            <OrphaCode>730892</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=730892</ExpertLink>
                            <Name lang="en">Ossifying fibromyxoid tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32994">
                            <OrphaCode>730256</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=730256</ExpertLink>
                            <Name lang="en">Low-grade fibromyxoid sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="33000">
                            <OrphaCode>730281</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=730281</ExpertLink>
                            <Name lang="en">Sclerosing epithelioid fibrosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8665">
                        <OrphaCode>873</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=873</ExpertLink>
                        <Name lang="en">Desmoid tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10777">
                        <OrphaCode>57782</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=57782</ExpertLink>
                        <Name lang="en">Mazabraud syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10885">
                        <OrphaCode>66627</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=66627</ExpertLink>
                        <Name lang="en">Tenosynovial giant cell tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12894">
                        <OrphaCode>97338</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97338</ExpertLink>
                        <Name lang="en">Melanoma of soft tissue</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17151">
                        <OrphaCode>157826</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=157826</ExpertLink>
                        <Name lang="en">Congenital epulis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18017">
                        <OrphaCode>178342</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178342</ExpertLink>
                        <Name lang="en">Inflammatory myofibroblastic tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19542">
                        <OrphaCode>247762</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247762</ExpertLink>
                        <Name lang="en">Lipoblastoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20759">
                        <OrphaCode>289685</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289685</ExpertLink>
                        <Name lang="en">Myopericytoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22636">
                        <OrphaCode>391651</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=391651</ExpertLink>
                        <Name lang="en">Glomus tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="25142">
                        <OrphaCode>477742</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=477742</ExpertLink>
                        <Name lang="en">Nodular fasciitis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="29725">
                        <OrphaCode>595133</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=595133</ExpertLink>
                        <Name lang="en">Perivascular epithelioid cell neoplasm</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="11412">
                    <OrphaCode>79386</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79386</ExpertLink>
                    <Name lang="en">Rare skin tumor or hamartoma</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="39">
                    <ClassificationNode>
                      <Disorder id="185">
                        <OrphaCode>636</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=636</ExpertLink>
                        <Name lang="en">Neurofibromatosis type 1</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="12945">
                            <OrphaCode>97685</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97685</ExpertLink>
                            <Name lang="en">17q11 microdeletion syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22341">
                            <OrphaCode>363700</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363700</ExpertLink>
                            <Name lang="en">Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="207">
                        <OrphaCode>377</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=377</ExpertLink>
                        <Name lang="en">Gorlin syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="660">
                        <OrphaCode>805</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=805</ExpertLink>
                        <Name lang="en">Tuberous sclerosis complex</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="807">
                        <OrphaCode>2800</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2800</ExpertLink>
                        <Name lang="en">Extramammary Paget disease</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="930">
                        <OrphaCode>638</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=638</ExpertLink>
                        <Name lang="en">Neurofibromatosis-Noonan syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1009">
                        <OrphaCode>113</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=113</ExpertLink>
                        <Name lang="en">Bazex-Dupré-Christol syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2784">
                        <OrphaCode>3110</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3110</ExpertLink>
                        <Name lang="en">Rombo syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3340">
                        <OrphaCode>542</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=542</ExpertLink>
                        <Name lang="en">Primary cutaneous lymphoma</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="17954">
                            <OrphaCode>171901</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171901</ExpertLink>
                            <Name lang="en">Primary cutaneous T-cell lymphoma</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="18048">
                                <OrphaCode>178548</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178548</ExpertLink>
                                <Name lang="en">Indolent primary cutaneous T-cell lymphoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="4">
                                <ClassificationNode>
                                  <Disorder id="3749">
                                    <OrphaCode>541</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=541</ExpertLink>
                                    <Name lang="en">Primary cutaneous CD30+ T-cell lymphoproliferative disease</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="13859">
                                        <OrphaCode>98842</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98842</ExpertLink>
                                        <Name lang="en">Lymphomatoid papulosis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="21147">
                                        <OrphaCode>300865</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300865</ExpertLink>
                                        <Name lang="en">Primary cutaneous anaplastic large cell lymphoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11772">
                                    <OrphaCode>86884</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86884</ExpertLink>
                                    <Name lang="en">Subcutaneous panniculitis-like T-cell lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18040">
                                    <OrphaCode>178522</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178522</ExpertLink>
                                    <Name lang="en">Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18054">
                                    <OrphaCode>178566</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178566</ExpertLink>
                                    <Name lang="en">Mycosis fungoides and variants</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="4">
                                    <ClassificationNode>
                                      <Disorder id="3400">
                                        <OrphaCode>2584</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2584</ExpertLink>
                                        <Name lang="en">Classic mycosis fungoides</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="10311">
                                        <OrphaCode>33111</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33111</ExpertLink>
                                        <Name lang="en">Granulomatous slack skin</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="18038">
                                        <OrphaCode>178512</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178512</ExpertLink>
                                        <Name lang="en">Folliculotropic mycosis fungoides</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="18039">
                                        <OrphaCode>178517</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178517</ExpertLink>
                                        <Name lang="en">Localized pagetoid reticulosis</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18049">
                                <OrphaCode>178551</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178551</ExpertLink>
                                <Name lang="en">Aggressive primary cutaneous T-cell lymphoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="6">
                                <ClassificationNode>
                                  <Disorder id="3401">
                                    <OrphaCode>3162</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3162</ExpertLink>
                                    <Name lang="en">Sézary syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11768">
                                    <OrphaCode>86875</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86875</ExpertLink>
                                    <Name lang="en">Adult T-cell leukemia/lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11769">
                                    <OrphaCode>86879</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86879</ExpertLink>
                                    <Name lang="en">Extranodal nasal NK/T cell lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11773">
                                    <OrphaCode>86885</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86885</ExpertLink>
                                    <Name lang="en">Primary cutaneous peripheral T-cell lymphoma not otherwise specified</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18042">
                                    <OrphaCode>178528</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178528</ExpertLink>
                                    <Name lang="en">Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18044">
                                    <OrphaCode>178533</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178533</ExpertLink>
                                    <Name lang="en">Primary cutaneous gamma/delta-positive T-cell lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18053">
                            <OrphaCode>178563</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178563</ExpertLink>
                            <Name lang="en">Primary cutaneous B-cell lymphoma</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="18050">
                                <OrphaCode>178554</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178554</ExpertLink>
                                <Name lang="en">Aggressive primary cutaneous B-cell lymphoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="1">
                                <ClassificationNode>
                                  <Disorder id="18047">
                                    <OrphaCode>178544</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178544</ExpertLink>
                                    <Name lang="en">Primary cutaneous diffuse large B-cell lymphoma, leg type</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18051">
                                <OrphaCode>178557</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178557</ExpertLink>
                                <Name lang="en">Indolent primary cutaneous B-cell lymphoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="18045">
                                    <OrphaCode>178536</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178536</ExpertLink>
                                    <Name lang="en">Primary cutaneous marginal zone B-cell lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18046">
                                    <OrphaCode>178540</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178540</ExpertLink>
                                    <Name lang="en">Primary cutaneous follicle center lymphoma</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="3545">
                        <OrphaCode>2591</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2591</ExpertLink>
                        <Name lang="en">Infantile myofibromatosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3560">
                        <OrphaCode>618</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=618</ExpertLink>
                        <Name lang="en">Familial melanoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8579">
                        <OrphaCode>492</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=492</ExpertLink>
                        <Name lang="en">Proliferating trichilemmal cyst</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8582">
                        <OrphaCode>840</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=840</ExpertLink>
                        <Name lang="en">Syringocystadenoma papilliferum</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8587">
                        <OrphaCode>864</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=864</ExpertLink>
                        <Name lang="en">Trichofolliculoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <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="8645">
                        <OrphaCode>493</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=493</ExpertLink>
                        <Name lang="en">Familial keratoacanthoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8649">
                        <OrphaCode>523</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=523</ExpertLink>
                        <Name lang="en">Hereditary leiomyomatosis and renal cell cancer</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="9285">
                        <OrphaCode>31112</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=31112</ExpertLink>
                        <Name lang="en">Dermatofibrosarcoma protuberans</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10741">
                        <OrphaCode>53715</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=53715</ExpertLink>
                        <Name lang="en">Familial tumoral calcinosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="21245">
                            <OrphaCode>306658</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306658</ExpertLink>
                            <Name lang="en">Familial normophosphatemic tumoral calcinosis</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21246">
                            <OrphaCode>306661</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306661</ExpertLink>
                            <Name lang="en">Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10877">
                        <OrphaCode>65748</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=65748</ExpertLink>
                        <Name lang="en">Multiple self-healing squamous epithelioma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="11166">
                        <OrphaCode>79140</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79140</ExpertLink>
                        <Name lang="en">Cutaneous neuroendocrine carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="11519">
                        <OrphaCode>79493</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79493</ExpertLink>
                        <Name lang="en">Brooke-Spiegler syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="8629">
                            <OrphaCode>211</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211</ExpertLink>
                            <Name lang="en">Familial cylindromatosis</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="8659">
                            <OrphaCode>867</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=867</ExpertLink>
                            <Name lang="en">Familial multiple trichoepithelioma</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12144">
                        <OrphaCode>91414</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91414</ExpertLink>
                        <Name lang="en">Pilomatrixoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17790">
                        <OrphaCode>168632</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168632</ExpertLink>
                        <Name lang="en">Generalized basaloid follicular hamartoma syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17811">
                        <OrphaCode>168999</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168999</ExpertLink>
                        <Name lang="en">Malignant melanoma of the mucosa</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18383">
                        <OrphaCode>199257</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=199257</ExpertLink>
                        <Name lang="en">Superficial fibromatosis</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="18382">
                            <OrphaCode>199251</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=199251</ExpertLink>
                            <Name lang="en">Ledderhose disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18384">
                            <OrphaCode>199260</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=199260</ExpertLink>
                            <Name lang="en">Calcifying aponeurotic fibroma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18385">
                            <OrphaCode>199267</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=199267</ExpertLink>
                            <Name lang="en">Infantile digital fibromatosis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20054">
                        <OrphaCode>263435</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263435</ExpertLink>
                        <Name lang="en">Congenital smooth muscle hamartoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20370">
                        <OrphaCode>276280</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276280</ExpertLink>
                        <Name lang="en">Hemihyperplasia-multiple lipomatosis syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20905">
                        <OrphaCode>294057</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=294057</ExpertLink>
                        <Name lang="en">Rare nevus</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="26">
                        <ClassificationNode>
                          <Disorder id="243">
                            <OrphaCode>201</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=201</ExpertLink>
                            <Name lang="en">Cowden syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="370">
                            <OrphaCode>626</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=626</ExpertLink>
                            <Name lang="en">Large/giant congenital melanocytic nevus</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="549">
                            <OrphaCode>2612</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2612</ExpertLink>
                            <Name lang="en">Linear nevus sebaceus syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="565">
                            <OrphaCode>744</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=744</ExpertLink>
                            <Name lang="en">Proteus syndrome</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2136">
                            <OrphaCode>139</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=139</ExpertLink>
                            <Name lang="en">CHILD syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2294">
                            <OrphaCode>2481</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2481</ExpertLink>
                            <Name lang="en">Neurocutaneous melanocytosis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2605">
                            <OrphaCode>2874</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2874</ExpertLink>
                            <Name lang="en">Phakomatosis pigmentokeratotica</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2675">
                            <OrphaCode>2969</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2969</ExpertLink>
                            <Name lang="en">Proteus-like syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3630">
                            <OrphaCode>2611</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2611</ExpertLink>
                            <Name lang="en">Linear verrucous nevus syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="11492">
                                <OrphaCode>79466</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79466</ExpertLink>
                                <Name lang="en">Inflammatory linear verrucous epidermal nevus</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11493">
                                <OrphaCode>79467</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79467</ExpertLink>
                                <Name lang="en">Verrucous nevus</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11494">
                                <OrphaCode>79468</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79468</ExpertLink>
                                <Name lang="en">Acanthokeratolytic verrucous nevus</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10375">
                            <OrphaCode>35125</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=35125</ExpertLink>
                            <Name lang="en">Epidermal nevus syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10858">
                            <OrphaCode>64754</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=64754</ExpertLink>
                            <Name lang="en">Nevus comedonicus syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10859">
                            <OrphaCode>64755</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=64755</ExpertLink>
                            <Name lang="en">Becker nevus syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="16690">
                            <OrphaCode>137608</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137608</ExpertLink>
                            <Name lang="en">Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="16889">
                            <OrphaCode>139414</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=139414</ExpertLink>
                            <Name lang="en">Congenital panfollicular nevus</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17004">
                            <OrphaCode>140944</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=140944</ExpertLink>
                            <Name lang="en">CLOVES syndrome</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17629">
                            <OrphaCode>166286</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=166286</ExpertLink>
                            <Name lang="en">Porokeratotic eccrine ostial and dermal duct nevus</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17935">
                            <OrphaCode>171723</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171723</ExpertLink>
                            <Name lang="en">White sponge nevus</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20052">
                            <OrphaCode>263425</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263425</ExpertLink>
                            <Name lang="en">Nevus of Ota</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20053">
                            <OrphaCode>263432</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263432</ExpertLink>
                            <Name lang="en">Nevus of Ito</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21465">
                            <OrphaCode>313936</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=313936</ExpertLink>
                            <Name lang="en">PENS syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22469">
                            <OrphaCode>370039</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370039</ExpertLink>
                            <Name lang="en">Angora hair nevus</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22471">
                            <OrphaCode>370046</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370046</ExpertLink>
                            <Name lang="en">Didymosis aplasticosebacea</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22472">
                            <OrphaCode>370052</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370052</ExpertLink>
                            <Name lang="en">SCALP syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22473">
                            <OrphaCode>370059</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370059</ExpertLink>
                            <Name lang="en">NEVADA syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="25865">
                            <OrphaCode>497737</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=497737</ExpertLink>
                            <Name lang="en">Epidermolytic nevus</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="25866">
                            <OrphaCode>497757</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=497757</ExpertLink>
                            <Name lang="en">MME-related autosomal dominant Charcot Marie Tooth disease type 2</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21124">
                        <OrphaCode>300515</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300515</ExpertLink>
                        <Name lang="en">Rare nail tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="21122">
                            <OrphaCode>300504</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300504</ExpertLink>
                            <Name lang="en">Onychocytic matricoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21123">
                            <OrphaCode>300512</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300512</ExpertLink>
                            <Name lang="en">Onychomatricoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21218">
                        <OrphaCode>306498</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306498</ExpertLink>
                        <Name lang="en">PTEN hamartoma tumor syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="243">
                            <OrphaCode>201</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=201</ExpertLink>
                            <Name lang="en">Cowden syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="1473">
                            <OrphaCode>109</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=109</ExpertLink>
                            <Name lang="en">Bannayan-Riley-Ruvalcaba syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2675">
                            <OrphaCode>2969</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2969</ExpertLink>
                            <Name lang="en">Proteus-like syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10867">
                            <OrphaCode>65285</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=65285</ExpertLink>
                            <Name lang="en">Lhermitte-Duclos disease</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="16690">
                            <OrphaCode>137608</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137608</ExpertLink>
                            <Name lang="en">Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22939">
                        <OrphaCode>404560</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404560</ExpertLink>
                        <Name lang="en">Familial atypical multiple mole melanoma syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23033">
                        <OrphaCode>411777</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=411777</ExpertLink>
                        <Name lang="en">Generalized eruptive keratoacanthoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="25964">
                        <OrphaCode>499182</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=499182</ExpertLink>
                        <Name lang="en">Pilomatrix carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="27945">
                        <OrphaCode>538756</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=538756</ExpertLink>
                        <Name lang="en">Familial multiple discoid fibromas</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="28622">
                        <OrphaCode>569164</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=569164</ExpertLink>
                        <Name lang="en">Angiomatoid fibrous histiocytoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32080">
                        <OrphaCode>673525</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673525</ExpertLink>
                        <Name lang="en">Intravascular papillary endothelial hyperplasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32086">
                        <OrphaCode>673568</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673568</ExpertLink>
                        <Name lang="en">Eccrine angiomatous hamartoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32833">
                        <OrphaCode>723286</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=723286</ExpertLink>
                        <Name lang="en">Cutaneous epithelioid angiomatous nodule</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2225">
                        <OrphaCode>2396</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2396</ExpertLink>
                        <Name lang="en">Encephalocraniocutaneous lipomatosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="12451">
                    <OrphaCode>93619</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93619</ExpertLink>
                    <Name lang="en">Rare renal tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="7">
                    <ClassificationNode>
                      <Disorder id="803">
                        <OrphaCode>2665</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2665</ExpertLink>
                        <Name lang="en">Congenital mesoblastic nephroma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="852">
                        <OrphaCode>654</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=654</ExpertLink>
                        <Name lang="en">Nephroblastoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2022">
                        <OrphaCode>2111</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2111</ExpertLink>
                        <Name lang="en">Cystic hamartoma of lung and kidney</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12917">
                        <OrphaCode>97366</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97366</ExpertLink>
                        <Name lang="en">Multiloculated renal cyst</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18821">
                        <OrphaCode>217071</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217071</ExpertLink>
                        <Name lang="en">Renal cell carcinoma</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="9">
                        <ClassificationNode>
                          <Disorder id="19512">
                            <OrphaCode>247203</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247203</ExpertLink>
                            <Name lang="en">Collecting duct carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21639">
                            <OrphaCode>319276</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319276</ExpertLink>
                            <Name lang="en">Clear cell renal carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="21640">
                                <OrphaCode>319287</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319287</ExpertLink>
                                <Name lang="en">Multilocular cystic renal neoplasm of low malignant potential</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22933">
                                <OrphaCode>404511</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404511</ExpertLink>
                                <Name lang="en">Clear cell papillary renal cell carcinoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21641">
                            <OrphaCode>319298</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319298</ExpertLink>
                            <Name lang="en">Papillary renal cell carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21642">
                            <OrphaCode>319303</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319303</ExpertLink>
                            <Name lang="en">Chromophobe renal cell carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21643">
                            <OrphaCode>319308</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319308</ExpertLink>
                            <Name lang="en">MiT family translocation renal cell carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21645">
                            <OrphaCode>319319</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319319</ExpertLink>
                            <Name lang="en">Renal medullary carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21646">
                            <OrphaCode>319322</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319322</ExpertLink>
                            <Name lang="en">Mucinous tubular and spindle cell renal carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21647">
                            <OrphaCode>319325</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319325</ExpertLink>
                            <Name lang="en">Tubulocystic renal cell carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22934">
                            <OrphaCode>404514</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404514</ExpertLink>
                            <Name lang="en">Acquired cystic disease-associated renal cell carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23715">
                        <OrphaCode>457246</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=457246</ExpertLink>
                        <Name lang="en">Clear cell sarcoma of kidney</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="24022">
                        <OrphaCode>464359</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=464359</ExpertLink>
                        <Name lang="en">Benign metanephric tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="13077">
                    <OrphaCode>98059</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98059</ExpertLink>
                    <Name lang="en">Rare digestive tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="6">
                    <ClassificationNode>
                      <Disorder id="14879">
                        <OrphaCode>101943</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101943</ExpertLink>
                        <Name lang="en">Rare hepatic and biliary tract tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="21240">
                            <OrphaCode>306633</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306633</ExpertLink>
                            <Name lang="en">Rare tumor of gallbladder and extrahepatic biliary tract</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="10765">
                                <OrphaCode>56044</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=56044</ExpertLink>
                                <Name lang="en">Carcinoma of gallbladder and extrahepatic biliary tract</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="10951">
                                    <OrphaCode>70567</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70567</ExpertLink>
                                    <Name lang="en">Cholangiocarcinoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14551">
                                    <OrphaCode>99978</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99978</ExpertLink>
                                    <Name lang="en">Perihilar cholangiocarcinoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23206">
                                    <OrphaCode>424991</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424991</ExpertLink>
                                    <Name lang="en">Adenocarcinoma of the gallbladder and extrahepatic biliary tract</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23207">
                                    <OrphaCode>424996</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424996</ExpertLink>
                                    <Name lang="en">Squamous cell carcinoma of gallbladder and extrahepatic biliary tract</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="27629">
                                    <OrphaCode>529852</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=529852</ExpertLink>
                                    <Name lang="en">Combined hepatocellular carcinoma and cholangiocarcinoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14658">
                                <OrphaCode>100086</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100086</ExpertLink>
                                <Name lang="en">Gallbladder neuroendocrine tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21241">
                            <OrphaCode>306636</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306636</ExpertLink>
                            <Name lang="en">Rare tumor of liver and intrahepatic biliary tract</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="7">
                            <ClassificationNode>
                              <Disorder id="836">
                                <OrphaCode>449</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=449</ExpertLink>
                                <Name lang="en">Hepatoblastoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8705">
                                <OrphaCode>386</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=386</ExpertLink>
                                <Name lang="en">Hepatic cystic hamartoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10752">
                                <OrphaCode>54272</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=54272</ExpertLink>
                                <Name lang="en">Hepatocellular adenoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14608">
                                <OrphaCode>100035</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100035</ExpertLink>
                                <Name lang="en">Solitary necrotic nodule of the liver</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18012">
                                <OrphaCode>178315</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178315</ExpertLink>
                                <Name lang="en">Undifferentiated embryonal sarcoma of the liver</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23200">
                                <OrphaCode>424933</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424933</ExpertLink>
                                <Name lang="en">Rare malignant epithelial tumor of liver and intrahepatic biliary tract</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14657">
                                    <OrphaCode>100085</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100085</ExpertLink>
                                    <Name lang="en">Primary hepatic neuroendocrine carcinoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23201">
                                    <OrphaCode>424936</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424936</ExpertLink>
                                    <Name lang="en">Carcinoma of liver and intrahepatic biliary tract</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="8">
                                    <ClassificationNode>
                                      <Disorder id="10951">
                                        <OrphaCode>70567</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70567</ExpertLink>
                                        <Name lang="en">Cholangiocarcinoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="11824">
                                        <OrphaCode>88673</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=88673</ExpertLink>
                                        <Name lang="en">Hepatocellular carcinoma</Name>
                                        <DisorderType id="21436">
                                          <Name lang="en">Clinical group</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="10320">
                                            <OrphaCode>33402</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33402</ExpertLink>
                                            <Name lang="en">Pediatric hepatocellular carcinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="18690">
                                            <OrphaCode>210159</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=210159</ExpertLink>
                                            <Name lang="en">Adult hepatocellular carcinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="22851">
                                        <OrphaCode>401920</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=401920</ExpertLink>
                                        <Name lang="en">Fibrolamellar hepatocellular carcinoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="23202">
                                        <OrphaCode>424943</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424943</ExpertLink>
                                        <Name lang="en">Adenocarcinoma of the liver and intrahepatic biliary tract</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="23203">
                                        <OrphaCode>424970</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424970</ExpertLink>
                                        <Name lang="en">Undifferentiated carcinoma of liver and intrahepatic biliary tract</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="23204">
                                        <OrphaCode>424975</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424975</ExpertLink>
                                        <Name lang="en">Squamous cell carcinoma of liver and intrahepatic biliary tract</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="23205">
                                        <OrphaCode>424982</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424982</ExpertLink>
                                        <Name lang="en">Biliary cystadenocarcinoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="27629">
                                        <OrphaCode>529852</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=529852</ExpertLink>
                                        <Name lang="en">Combined hepatocellular carcinoma and cholangiocarcinoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28552">
                                <OrphaCode>566841</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=566841</ExpertLink>
                                <Name lang="en">Liver adenomatosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="15002">
                        <OrphaCode>104011</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=104011</ExpertLink>
                        <Name lang="en">Rare tumor of intestine</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="23171">
                            <OrphaCode>423793</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423793</ExpertLink>
                            <Name lang="en">Rare tumor of small intestine</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="11770">
                                <OrphaCode>86880</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86880</ExpertLink>
                                <Name lang="en">Enteropathy-associated T-cell lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23172">
                                <OrphaCode>423798</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423798</ExpertLink>
                                <Name lang="en">Mesenchymal tumor of small intestine</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="10584">
                                    <OrphaCode>44890</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=44890</ExpertLink>
                                    <Name lang="en">Gastrointestinal stromal tumor</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="15006">
                                    <OrphaCode>104076</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=104076</ExpertLink>
                                    <Name lang="en">Leiomyosarcoma of small intestine</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23210">
                                <OrphaCode>425368</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=425368</ExpertLink>
                                <Name lang="en">Rare epithelial tumor of small intestine</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="23175">
                                    <OrphaCode>423957</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423957</ExpertLink>
                                    <Name lang="en">Rare carcinoma of small intestine</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="15005">
                                        <OrphaCode>104075</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=104075</ExpertLink>
                                        <Name lang="en">Adenocarcinoma of the small intestine</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="23176">
                                        <OrphaCode>423968</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423968</ExpertLink>
                                        <Name lang="en">Squamous cell carcinoma of the small intestine</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23177">
                                    <OrphaCode>423975</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423975</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of the small intestine</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="3">
                                    <ClassificationNode>
                                      <Disorder id="14648">
                                        <OrphaCode>100076</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100076</ExpertLink>
                                        <Name lang="en">Duodenal neuroendocrine tumor</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="3595">
                                            <OrphaCode>913</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=913</ExpertLink>
                                            <Name lang="en">Zollinger-Ellison syndrome</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12878">
                                            <OrphaCode>97283</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97283</ExpertLink>
                                            <Name lang="en">Somatostatinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14649">
                                        <OrphaCode>100077</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100077</ExpertLink>
                                        <Name lang="en">Jejunal neuroendocrine tumor</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="1">
                                        <ClassificationNode>
                                          <Disorder id="12878">
                                            <OrphaCode>97283</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97283</ExpertLink>
                                            <Name lang="en">Somatostatinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14650">
                                        <OrphaCode>100078</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100078</ExpertLink>
                                        <Name lang="en">Ileal neuroendocrine tumor</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="31900">
                                <OrphaCode>652658</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652658</ExpertLink>
                                <Name lang="en">Monomorphic epitheliotropic intestinal T-cell lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23178">
                            <OrphaCode>423982</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423982</ExpertLink>
                            <Name lang="en">Epithelial tumor of the appendix</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="14651">
                                <OrphaCode>100079</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100079</ExpertLink>
                                <Name lang="en">Neuroendocrine neoplasm of appendix</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="21952">
                                    <OrphaCode>329977</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=329977</ExpertLink>
                                    <Name lang="en">Classic neuroendocrine tumor of appendix</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21953">
                                    <OrphaCode>329984</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=329984</ExpertLink>
                                    <Name lang="en">Goblet cell carcinoma</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22644">
                                <OrphaCode>391723</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=391723</ExpertLink>
                                <Name lang="en">Mucinous adenocarcinoma of the appendix</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32863">
                                <OrphaCode>725964</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=725964</ExpertLink>
                                <Name lang="en">Appendiceal mucinous neoplasm</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="32865">
                                    <OrphaCode>725992</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=725992</ExpertLink>
                                    <Name lang="en">High-grade appendiceal mucinous neoplasm</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32864">
                                    <OrphaCode>725984</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=725984</ExpertLink>
                                    <Name lang="en">Low-grade appendiceal mucinous neoplasm</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23179">
                            <OrphaCode>423991</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423991</ExpertLink>
                            <Name lang="en">Rare epithelial tumor of colon</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="14652">
                                <OrphaCode>100080</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100080</ExpertLink>
                                <Name lang="en">Neuroendocrine tumor of the colon</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23180">
                                <OrphaCode>423994</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423994</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the colon</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23181">
                            <OrphaCode>423998</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423998</ExpertLink>
                            <Name lang="en">Rare epithelial tumor of rectum</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="14653">
                                <OrphaCode>100081</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100081</ExpertLink>
                                <Name lang="en">Neuroendocrine tumor of the rectum</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23182">
                                <OrphaCode>424002</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424002</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the rectum</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23183">
                            <OrphaCode>424010</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424010</ExpertLink>
                            <Name lang="en">Epithelial tumor of anal canal</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="14654">
                                <OrphaCode>100082</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100082</ExpertLink>
                                <Name lang="en">Neuroendocrine tumor of anal canal</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23184">
                                <OrphaCode>424013</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424013</ExpertLink>
                                <Name lang="en">Carcinoma of the anal canal</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="23185">
                                    <OrphaCode>424016</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424016</ExpertLink>
                                    <Name lang="en">Adenocarcinoma of the anal canal</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23186">
                                    <OrphaCode>424019</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424019</ExpertLink>
                                    <Name lang="en">Squamous cell carcinoma of the anal canal</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="18160">
                        <OrphaCode>180821</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180821</ExpertLink>
                        <Name lang="en">Rare gastroesophageal tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="10824">
                            <OrphaCode>63443</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=63443</ExpertLink>
                            <Name lang="en">Rare epithelial tumor of stomach</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="14647">
                                <OrphaCode>100075</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100075</ExpertLink>
                                <Name lang="en">Neuroendocrine tumor of stomach</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23167">
                                <OrphaCode>423771</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423771</ExpertLink>
                                <Name lang="en">Rare carcinoma of stomach</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="10415">
                                    <OrphaCode>36273</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=36273</ExpertLink>
                                    <Name lang="en">Gastric linitis plastica</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21464">
                                    <OrphaCode>313920</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=313920</ExpertLink>
                                    <Name lang="en">Epstein-Barr virus-associated gastric carcinoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23090">
                                    <OrphaCode>418959</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=418959</ExpertLink>
                                    <Name lang="en">Squamous cell carcinoma of the stomach</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23168">
                                    <OrphaCode>423776</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423776</ExpertLink>
                                    <Name lang="en">Hereditary gastric cancer</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="8758">
                                        <OrphaCode>26106</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=26106</ExpertLink>
                                        <Name lang="en">Hereditary diffuse gastric cancer</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="21470">
                                        <OrphaCode>314022</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314022</ExpertLink>
                                        <Name lang="en">Gastric adenocarcinoma and proximal polyposis of the stomach</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23170">
                                    <OrphaCode>423786</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423786</ExpertLink>
                                    <Name lang="en">Undifferentiated carcinoma of stomach</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="24048">
                                <OrphaCode>464756</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=464756</ExpertLink>
                                <Name lang="en">Familial gastric type 1 neuroendocrine tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10950">
                            <OrphaCode>70482</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70482</ExpertLink>
                            <Name lang="en">Carcinoma of esophagus</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="14549">
                                <OrphaCode>99976</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99976</ExpertLink>
                                <Name lang="en">Adenocarcinoma of the oesophagus and oesophagogastric junction</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14550">
                                <OrphaCode>99977</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99977</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the esophagus</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23088">
                                <OrphaCode>418945</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=418945</ExpertLink>
                                <Name lang="en">Carcinoma of esophagus, salivary gland type</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23089">
                                <OrphaCode>418951</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=418951</ExpertLink>
                                <Name lang="en">Undifferentiated carcinoma of esophagus</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="26440">
                            <OrphaCode>506136</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506136</ExpertLink>
                            <Name lang="en">Neuroendocrine neoplasm of esophagus</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18161">
                        <OrphaCode>180824</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180824</ExpertLink>
                        <Name lang="en">Rare tumor of pancreas</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="23188">
                            <OrphaCode>424033</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424033</ExpertLink>
                            <Name lang="en">Rare epithelial tumor of pancreas</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="5">
                            <ClassificationNode>
                              <Disorder id="844">
                                <OrphaCode>677</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=677</ExpertLink>
                                <Name lang="en">Pancreatoblastoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="12229">
                                <OrphaCode>93292</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93292</ExpertLink>
                                <Name lang="en">Adenoma of pancreas</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18822">
                                <OrphaCode>217074</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217074</ExpertLink>
                                <Name lang="en">Rare carcinoma of pancreas</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="8">
                                <ClassificationNode>
                                  <Disorder id="3708">
                                    <OrphaCode>1333</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1333</ExpertLink>
                                    <Name lang="en">Familial pancreatic carcinoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23189">
                                    <OrphaCode>424039</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424039</ExpertLink>
                                    <Name lang="en">Squamous cell carcinoma of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23190">
                                    <OrphaCode>424046</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424046</ExpertLink>
                                    <Name lang="en">Acinar cell carcinoma of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23191">
                                    <OrphaCode>424053</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424053</ExpertLink>
                                    <Name lang="en">Mucinous cystadenocarcinoma of the pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23192">
                                    <OrphaCode>424058</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424058</ExpertLink>
                                    <Name lang="en">Intraductal papillary mucinous carcinoma of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23193">
                                    <OrphaCode>424065</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424065</ExpertLink>
                                    <Name lang="en">Pancreatic solid pseudopapillary neoplasm</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23194">
                                    <OrphaCode>424073</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424073</ExpertLink>
                                    <Name lang="en">Serous cystadenocarcinoma of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23195">
                                    <OrphaCode>424080</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=424080</ExpertLink>
                                    <Name lang="en">Undifferentiated carcinoma with osteoclast-like giant cells of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="26433">
                                <OrphaCode>506052</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506052</ExpertLink>
                                <Name lang="en">Neuroendocrine neoplasm of pancreas</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="12870">
                                    <OrphaCode>97253</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97253</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of pancreas</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="26434">
                                        <OrphaCode>506060</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506060</ExpertLink>
                                        <Name lang="en">Functioning neuroendocrine tumor of pancreas</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="9">
                                        <ClassificationNode>
                                          <Disorder id="3595">
                                            <OrphaCode>913</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=913</ExpertLink>
                                            <Name lang="en">Zollinger-Ellison syndrome</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12871">
                                            <OrphaCode>97261</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97261</ExpertLink>
                                            <Name lang="en">GRFoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12874">
                                            <OrphaCode>97278</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97278</ExpertLink>
                                            <Name lang="en">PPoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12875">
                                            <OrphaCode>97279</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97279</ExpertLink>
                                            <Name lang="en">Insulinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12876">
                                            <OrphaCode>97280</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97280</ExpertLink>
                                            <Name lang="en">Glucagonoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12877">
                                            <OrphaCode>97282</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97282</ExpertLink>
                                            <Name lang="en">VIPoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12878">
                                            <OrphaCode>97283</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97283</ExpertLink>
                                            <Name lang="en">Somatostatinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="14462">
                                            <OrphaCode>99889</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99889</ExpertLink>
                                            <Name lang="en">Cushing syndrome due to ectopic ACTH secretion</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="26436">
                                            <OrphaCode>506090</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506090</ExpertLink>
                                            <Name lang="en">Serotonin-producing neuroendocrine tumor of pancreas</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="26435">
                                        <OrphaCode>506075</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506075</ExpertLink>
                                        <Name lang="en">Non-functioning neuroendocrine tumor of pancreas</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="26437">
                                    <OrphaCode>506098</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506098</ExpertLink>
                                    <Name lang="en">Neuroendocrine carcinoma of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="26438">
                                    <OrphaCode>506112</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506112</ExpertLink>
                                    <Name lang="en">Mixed neuroendocrine and non-neuroendocrine neoplasm of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28919">
                                <OrphaCode>580572</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=580572</ExpertLink>
                                <Name lang="en">Intraductal tubulopapillary neoplasm of pancreas</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23373">
                            <OrphaCode>438274</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=438274</ExpertLink>
                            <Name lang="en">GCGR-related hyperglucagonemia</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20347">
                        <OrphaCode>276142</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276142</ExpertLink>
                        <Name lang="en">Rare tumor of salivary glands</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="20348">
                            <OrphaCode>276145</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276145</ExpertLink>
                            <Name lang="en">Malignant epithelial tumor of salivary glands</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20349">
                            <OrphaCode>276148</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276148</ExpertLink>
                            <Name lang="en">Benign epithelial tumor of salivary glands</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21130">
                        <OrphaCode>300557</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300557</ExpertLink>
                        <Name lang="en">Carcinoma of the ampulla of Vater</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </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="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="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="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="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="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="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="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 tumor of the pleura</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 tumor of the pleura</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <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>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="13080">
                    <OrphaCode>98062</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98062</ExpertLink>
                    <Name lang="en">Rare nervous system tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="8">
                    <ClassificationNode>
                      <Disorder id="10593">
                        <OrphaCode>46135</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=46135</ExpertLink>
                        <Name lang="en">Primary central nervous system lymphoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10756">
                        <OrphaCode>54595</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=54595</ExpertLink>
                        <Name lang="en">Craniopharyngioma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19647">
                        <OrphaCode>251558</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251558</ExpertLink>
                        <Name lang="en">Rare tumor of neuroepithelial tissue</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="18203">
                            <OrphaCode>182067</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182067</ExpertLink>
                            <Name lang="en">Glial tumor</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="6">
                            <ClassificationNode>
                              <Disorder id="32704">
                                <OrphaCode>717268</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717268</ExpertLink>
                                <Name lang="en">Circumscribed astrocytic glioma</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="6">
                                <ClassificationNode>
                                  <Disorder id="19661">
                                    <OrphaCode>251618</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251618</ExpertLink>
                                    <Name lang="en">Subependymal giant cell astrocytoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19676">
                                    <OrphaCode>251679</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251679</ExpertLink>
                                    <Name lang="en">Astroblastoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32628">
                                    <OrphaCode>715721</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715721</ExpertLink>
                                    <Name lang="en">High-grade astrocytoma with piloid features</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19675">
                                    <OrphaCode>251674</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251674</ExpertLink>
                                    <Name lang="en">Chordoid glioma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19658">
                                    <OrphaCode>251607</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251607</ExpertLink>
                                    <Name lang="en">Pleomorphic xanthoastrocytoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19659">
                                    <OrphaCode>251612</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251612</ExpertLink>
                                    <Name lang="en">Pilocytic astrocytoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="3">
                                    <ClassificationNode>
                                      <Disorder id="19660">
                                        <OrphaCode>251615</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251615</ExpertLink>
                                        <Name lang="en">Pilomyxoid astrocytoma</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32088">
                                        <OrphaCode>673580</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673580</ExpertLink>
                                        <Name lang="en">Classic pilocytic astrocytoma</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32089">
                                        <OrphaCode>673585</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673585</ExpertLink>
                                        <Name lang="en">Pilocytic astrocytoma with histological features of anaplasia</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3750">
                                <OrphaCode>301</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=301</ExpertLink>
                                <Name lang="en">Ependymal tumor</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="19666">
                                    <OrphaCode>251636</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251636</ExpertLink>
                                    <Name lang="en">Ependymoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19667">
                                    <OrphaCode>251639</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251639</ExpertLink>
                                    <Name lang="en">Subependymoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19668">
                                    <OrphaCode>251643</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251643</ExpertLink>
                                    <Name lang="en">Myxopapillary ependymoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19669">
                                    <OrphaCode>251646</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251646</ExpertLink>
                                    <Name lang="en">Anaplastic ependymoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="27668">
                                    <OrphaCode>530792</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=530792</ExpertLink>
                                    <Name lang="en">RELA fusion-positive ependymoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3754">
                                <OrphaCode>94</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=94</ExpertLink>
                                <Name lang="en">Astrocytoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="19648">
                                    <OrphaCode>251561</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251561</ExpertLink>
                                    <Name lang="en">High-grade astrocytoma</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="8">
                                    <ClassificationNode>
                                      <Disorder id="3752">
                                        <OrphaCode>360</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=360</ExpertLink>
                                        <Name lang="en">Glioblastoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="19649">
                                            <OrphaCode>251576</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251576</ExpertLink>
                                            <Name lang="en">Gliosarcoma</Name>
                                            <DisorderType id="21457">
                                              <Name lang="en">Histopathological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="19650">
                                            <OrphaCode>251579</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251579</ExpertLink>
                                            <Name lang="en">Giant cell glioblastoma</Name>
                                            <DisorderType id="21457">
                                              <Name lang="en">Histopathological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="19651">
                                        <OrphaCode>251582</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251582</ExpertLink>
                                        <Name lang="en">Gliomatosis cerebri</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="19652">
                                        <OrphaCode>251589</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251589</ExpertLink>
                                        <Name lang="en">Astrocytoma grade 3</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32837">
                                        <OrphaCode>723358</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=723358</ExpertLink>
                                        <Name lang="en">Diffuse midline glioma, H3 K27-altered</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32294">
                                        <OrphaCode>695136</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=695136</ExpertLink>
                                        <Name lang="en">Infant-type hemispheric glioma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="5">
                                        <ClassificationNode>
                                          <Disorder id="32621">
                                            <OrphaCode>715694</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715694</ExpertLink>
                                            <Name lang="en">Infant-type hemispheric glioma NTRK-altered</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="32622">
                                            <OrphaCode>715697</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715697</ExpertLink>
                                            <Name lang="en">Infant-type hemispheric glioma ALK-altered</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="32623">
                                            <OrphaCode>715701</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715701</ExpertLink>
                                            <Name lang="en">Infant-type hemispheric glioma ROS1-altered</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="32624">
                                            <OrphaCode>715704</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715704</ExpertLink>
                                            <Name lang="en">Infant-type hemispheric glioma MET-altered</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="32987">
                                            <OrphaCode>730226</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=730226</ExpertLink>
                                            <Name lang="en">Infant-type hemispheric glioma, fusion-negative</Name>
                                            <DisorderType id="21443">
                                              <Name lang="en">Etiological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32629">
                                        <OrphaCode>715724</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715724</ExpertLink>
                                        <Name lang="en">Diffuse pediatric-type high-grade glioma-H3-wildtype-IDH-wildtype</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32639">
                                        <OrphaCode>715950</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715950</ExpertLink>
                                        <Name lang="en">Diffuse hemispheric glioma-H3 G34-mutant</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="32866">
                                        <OrphaCode>726004</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=726004</ExpertLink>
                                        <Name lang="en">Astrocytoma grade 4</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19653">
                                    <OrphaCode>251592</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251592</ExpertLink>
                                    <Name lang="en">Low-grade astrocytoma</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="19654">
                                        <OrphaCode>251595</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251595</ExpertLink>
                                        <Name lang="en">Astrocytoma grade 2</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="3">
                                        <ClassificationNode>
                                          <Disorder id="19655">
                                            <OrphaCode>251598</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251598</ExpertLink>
                                            <Name lang="en">Protoplasmic astrocytoma</Name>
                                            <DisorderType id="21457">
                                              <Name lang="en">Histopathological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="19656">
                                            <OrphaCode>251601</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251601</ExpertLink>
                                            <Name lang="en">Fibrillary astrocytoma</Name>
                                            <DisorderType id="21457">
                                              <Name lang="en">Histopathological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="19657">
                                            <OrphaCode>251604</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251604</ExpertLink>
                                            <Name lang="en">Gemistocytic astrocytoma</Name>
                                            <DisorderType id="21457">
                                              <Name lang="en">Histopathological subtype</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="19662">
                                        <OrphaCode>251623</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251623</ExpertLink>
                                        <Name lang="en">Pituicytoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10595">
                                <OrphaCode>46484</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=46484</ExpertLink>
                                <Name lang="en">Oligodendroglial tumor</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="19663">
                                    <OrphaCode>251627</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251627</ExpertLink>
                                    <Name lang="en">Oligodendroglioma grade 2</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19664">
                                    <OrphaCode>251630</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251630</ExpertLink>
                                    <Name lang="en">Oligodendroglioma grade 3</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19670">
                                <OrphaCode>251651</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251651</ExpertLink>
                                <Name lang="en">Oligoastrocytic tumor</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="19671">
                                    <OrphaCode>251656</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251656</ExpertLink>
                                    <Name lang="en">Oligoastrocytoma, dual genotype</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19672">
                                    <OrphaCode>251663</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251663</ExpertLink>
                                    <Name lang="en">Anaplastic oligoastrocytoma, dual genotype</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19673">
                                <OrphaCode>251668</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251668</ExpertLink>
                                <Name lang="en">Glial tumor of neuroepithelial tissue with unknown origin</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="1">
                                <ClassificationNode>
                                  <Disorder id="19674">
                                    <OrphaCode>251671</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251671</ExpertLink>
                                    <Name lang="en">Angiocentric glioma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19679">
                            <OrphaCode>251852</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251852</ExpertLink>
                            <Name lang="en">Embryonal tumor of neuroepithelial tissue</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="3751">
                                <OrphaCode>616</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=616</ExpertLink>
                                <Name lang="en">Medulloblastoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="4">
                                <ClassificationNode>
                                  <Disorder id="19680">
                                    <OrphaCode>251855</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251855</ExpertLink>
                                    <Name lang="en">Anaplastic/large cell medulloblastoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19681">
                                    <OrphaCode>251858</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251858</ExpertLink>
                                    <Name lang="en">Medulloblastoma with extensive nodularity</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19682">
                                    <OrphaCode>251863</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251863</ExpertLink>
                                    <Name lang="en">Desmoplastic/nodular medulloblastoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19683">
                                    <OrphaCode>251867</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251867</ExpertLink>
                                    <Name lang="en">Classic medulloblastoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14539">
                                <OrphaCode>99966</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99966</ExpertLink>
                                <Name lang="en">Atypical teratoid rhabdoid tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19684">
                                <OrphaCode>251870</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251870</ExpertLink>
                                <Name lang="en">Central nervous system embryonal tumor</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="4">
                                <ClassificationNode>
                                  <Disorder id="19685">
                                    <OrphaCode>251877</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251877</ExpertLink>
                                    <Name lang="en">Ganglioneuroblastoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="31929">
                                    <OrphaCode>656417</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=656417</ExpertLink>
                                    <Name lang="en">Embryonal tumor with multilayered rosettes</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="548">
                                    <OrphaCode>635</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=635</ExpertLink>
                                    <Name lang="en">Neuroblastoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="3733">
                                    <OrphaCode>1957</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1957</ExpertLink>
                                    <Name lang="en">Esthesioneuroblastoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19689">
                            <OrphaCode>251896</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251896</ExpertLink>
                            <Name lang="en">Choroid plexus tumor</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="2550">
                                <OrphaCode>2807</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2807</ExpertLink>
                                <Name lang="en">Papilloma of choroid plexus</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19690">
                                <OrphaCode>251899</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251899</ExpertLink>
                                <Name lang="en">Choroid plexus carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19691">
                                <OrphaCode>251902</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251902</ExpertLink>
                                <Name lang="en">Atypical papilloma of choroid plexus</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19692">
                            <OrphaCode>251905</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251905</ExpertLink>
                            <Name lang="en">Pineal tumor of neuroepithelial tissue</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="19693">
                                <OrphaCode>251909</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251909</ExpertLink>
                                <Name lang="en">Pineoblastoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19694">
                                <OrphaCode>251912</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251912</ExpertLink>
                                <Name lang="en">Pineocytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19695">
                                <OrphaCode>251915</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251915</ExpertLink>
                                <Name lang="en">Papillary tumor of the pineal region</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19696">
                                <OrphaCode>251919</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251919</ExpertLink>
                                <Name lang="en">Pineal parenchymal tumor of intermediate differentiation</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19697">
                            <OrphaCode>251924</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251924</ExpertLink>
                            <Name lang="en">Neuronal tumor</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="11042">
                                <OrphaCode>73256</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=73256</ExpertLink>
                                <Name lang="en">Central neurocytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19698">
                                <OrphaCode>251927</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251927</ExpertLink>
                                <Name lang="en">Extraventricular neurocytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19699">
                                <OrphaCode>251931</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251931</ExpertLink>
                                <Name lang="en">Cerebellar liponeurocytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19700">
                            <OrphaCode>251934</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251934</ExpertLink>
                            <Name lang="en">Mixed neuronal-glial tumor</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="9">
                            <ClassificationNode>
                              <Disorder id="10867">
                                <OrphaCode>65285</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=65285</ExpertLink>
                                <Name lang="en">Lhermitte-Duclos disease</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19701">
                                <OrphaCode>251937</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251937</ExpertLink>
                                <Name lang="en">Gangliocytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19702">
                                <OrphaCode>251940</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251940</ExpertLink>
                                <Name lang="en">Desmoplastic infantile astrocytoma/ganglioglioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19703">
                                <OrphaCode>251946</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251946</ExpertLink>
                                <Name lang="en">Dysembryoplastic neuroepithelial tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19704">
                                <OrphaCode>251949</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251949</ExpertLink>
                                <Name lang="en">Ganglioglioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19705">
                                <OrphaCode>251957</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251957</ExpertLink>
                                <Name lang="en">Anaplastic ganglioglioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19706">
                                <OrphaCode>251962</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251962</ExpertLink>
                                <Name lang="en">Papillary glioneuronal tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19707">
                                <OrphaCode>251975</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251975</ExpertLink>
                                <Name lang="en">Rosette-forming glioneuronal tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19708">
                                <OrphaCode>251992</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251992</ExpertLink>
                                <Name lang="en">Ganglioneuroma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19709">
                        <OrphaCode>251995</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251995</ExpertLink>
                        <Name lang="en">Primary germ cell tumor of central nervous system</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="10632">
                            <OrphaCode>48736</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=48736</ExpertLink>
                            <Name lang="en">Embryonal carcinoma of the central nervous system</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12126">
                            <OrphaCode>91352</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91352</ExpertLink>
                            <Name lang="en">Germinoma of the central nervous system</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19710">
                            <OrphaCode>252006</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252006</ExpertLink>
                            <Name lang="en">Yolk sac tumor of central nervous system</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19711">
                            <OrphaCode>252015</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252015</ExpertLink>
                            <Name lang="en">Choriocarcinoma of the central nervous system</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19712">
                            <OrphaCode>252018</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252018</ExpertLink>
                            <Name lang="en">Teratoma of the central nervous system</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19713">
                            <OrphaCode>252021</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252021</ExpertLink>
                            <Name lang="en">Mixed germ cell tumor of central nervous system</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19714">
                        <OrphaCode>252025</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252025</ExpertLink>
                        <Name lang="en">Tumor of meninges</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="1030">
                            <OrphaCode>2495</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2495</ExpertLink>
                            <Name lang="en">Meningioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19715">
                            <OrphaCode>252028</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252028</ExpertLink>
                            <Name lang="en">Primary melanocytic tumor of central nervous system</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="19716">
                                <OrphaCode>252031</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252031</ExpertLink>
                                <Name lang="en">Diffuse leptomeningeal melanocytosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19717">
                                <OrphaCode>252046</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252046</ExpertLink>
                                <Name lang="en">Meningeal melanocytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19718">
                                <OrphaCode>252050</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252050</ExpertLink>
                                <Name lang="en">Primary melanoma of the central nervous system</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20073">
                            <OrphaCode>263662</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263662</ExpertLink>
                            <Name lang="en">Familial multiple meningioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19719">
                        <OrphaCode>252054</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252054</ExpertLink>
                        <Name lang="en">Hemangioblastoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19720">
                        <OrphaCode>252057</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252057</ExpertLink>
                        <Name lang="en">Tumor of cranial and spinal nerves</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="4">
                        <ClassificationNode>
                          <Disorder id="3418">
                            <OrphaCode>2086</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2086</ExpertLink>
                            <Name lang="en">Optic pathway glioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3737">
                            <OrphaCode>3148</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3148</ExpertLink>
                            <Name lang="en">Malignant peripheral nerve sheath tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="19722">
                                <OrphaCode>252128</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252128</ExpertLink>
                                <Name lang="en">Malignant peripheral nerve sheath tumor with perineurial differentiation</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19733">
                                <OrphaCode>252212</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252212</ExpertLink>
                                <Name lang="en">Malignant triton tumor</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11621">
                            <OrphaCode>85102</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=85102</ExpertLink>
                            <Name lang="en">Perineurioma</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="14575">
                                <OrphaCode>100002</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100002</ExpertLink>
                                <Name lang="en">Extraneural perineurioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14573">
                                    <OrphaCode>100000</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100000</ExpertLink>
                                    <Name lang="en">Reticular perineurioma</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14574">
                                    <OrphaCode>100001</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100001</ExpertLink>
                                    <Name lang="en">Sclerosing perineurioma</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14576">
                                <OrphaCode>100003</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100003</ExpertLink>
                                <Name lang="en">Intraneural perineurioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19723">
                            <OrphaCode>252131</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252131</ExpertLink>
                            <Name lang="en">Benign peripheral nerve sheath tumor</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="19727">
                                <OrphaCode>252164</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252164</ExpertLink>
                                <Name lang="en">Benign schwannoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="1">
                                <ClassificationNode>
                                  <Disorder id="19728">
                                    <OrphaCode>252175</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252175</ExpertLink>
                                    <Name lang="en">Vestibular schwannoma</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19729">
                                <OrphaCode>252183</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252183</ExpertLink>
                                <Name lang="en">Neurofibroma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21121">
                                <OrphaCode>300501</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300501</ExpertLink>
                                <Name lang="en">Painful orbital and systemic neurofibromas-marfanoid habitus syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="29460">
                                <OrphaCode>590539</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=590539</ExpertLink>
                                <Name lang="en">Isolated melanotic schwannoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20411">
                        <OrphaCode>279897</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=279897</ExpertLink>
                        <Name lang="en">Primary oculocerebral lymphoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="13081">
                    <OrphaCode>98063</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98063</ExpertLink>
                    <Name lang="en">Rare gynecological tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="6">
                    <ClassificationNode>
                      <Disorder id="807">
                        <OrphaCode>2800</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2800</ExpertLink>
                        <Name lang="en">Extramammary Paget disease</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18123">
                        <OrphaCode>180220</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180220</ExpertLink>
                        <Name lang="en">Rare uterine adnexal tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="12886">
                            <OrphaCode>97293</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97293</ExpertLink>
                            <Name lang="en">Rare benign ovarian tumor</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="7">
                            <ClassificationNode>
                              <Disorder id="18499">
                                <OrphaCode>206470</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=206470</ExpertLink>
                                <Name lang="en">Cystadenoma of childhood</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="28367">
                                    <OrphaCode>563666</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=563666</ExpertLink>
                                    <Name lang="en">Serous cystadenoma of childhood</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="28368">
                                    <OrphaCode>563671</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=563671</ExpertLink>
                                    <Name lang="en">Mucinous cystadenoma of childhood</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="28369">
                                    <OrphaCode>563676</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=563676</ExpertLink>
                                    <Name lang="en">Seromucinous cystadenoma of childhood</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21487">
                                <OrphaCode>314451</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314451</ExpertLink>
                                <Name lang="en">Meigs syndrome</Name>
                                <DisorderType id="21422">
                                  <Name lang="en">Clinical syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21488">
                                <OrphaCode>314459</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314459</ExpertLink>
                                <Name lang="en">Pseudo-Meigs syndrome</Name>
                                <DisorderType id="21422">
                                  <Name lang="en">Clinical syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21489">
                                <OrphaCode>314466</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314466</ExpertLink>
                                <Name lang="en">Atypical Meigs syndrome</Name>
                                <DisorderType id="21422">
                                  <Name lang="en">Clinical syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21490">
                                <OrphaCode>314473</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314473</ExpertLink>
                                <Name lang="en">Ovarian fibroma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21491">
                                <OrphaCode>314478</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314478</ExpertLink>
                                <Name lang="en">Ovarian fibrothecoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28626">
                                <OrphaCode>569248</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=569248</ExpertLink>
                                <Name lang="en">Microcystic stromal tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18129">
                            <OrphaCode>180237</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180237</ExpertLink>
                            <Name lang="en">Benign tumor of fallopian tubes</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18131">
                            <OrphaCode>180242</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180242</ExpertLink>
                            <Name lang="en">Malignant tumor of fallopian tubes</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18741">
                            <OrphaCode>213500</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213500</ExpertLink>
                            <Name lang="en">Rare ovarian cancer</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="22739">
                                <OrphaCode>398934</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398934</ExpertLink>
                                <Name lang="en">Malignant epithelial tumor of ovary</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="18742">
                                    <OrphaCode>213504</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213504</ExpertLink>
                                    <Name lang="en">Adenocarcinoma of ovary</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18743">
                                    <OrphaCode>213512</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213512</ExpertLink>
                                    <Name lang="en">Malignant mixed Müllerian tumor of the ovary</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22741">
                                    <OrphaCode>398961</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398961</ExpertLink>
                                    <Name lang="en">Mucinous adenocarcinoma of ovary</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22742">
                                    <OrphaCode>398971</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398971</ExpertLink>
                                    <Name lang="en">Clear cell adenocarcinoma of the ovary</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23658">
                                    <OrphaCode>454723</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=454723</ExpertLink>
                                    <Name lang="en">Endometrioid carcinoma of ovary</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22740">
                                <OrphaCode>398940</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398940</ExpertLink>
                                <Name lang="en">Malignant non-epithelial tumor of ovary</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="10400">
                                    <OrphaCode>35807</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=35807</ExpertLink>
                                    <Name lang="en">Malignant germ cell tumor of ovary</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="3">
                                    <ClassificationNode>
                                      <Disorder id="14485">
                                        <OrphaCode>99912</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99912</ExpertLink>
                                        <Name lang="en">Ovarian dysgerminoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="18518">
                                        <OrphaCode>206538</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=206538</ExpertLink>
                                        <Name lang="en">Malignant non-dysgerminomatous germ cell tumor of ovary</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="20713">
                                        <OrphaCode>289356</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289356</ExpertLink>
                                        <Name lang="en">Primary non-gestational choriocarcinoma of ovary</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="10401">
                                    <OrphaCode>35808</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=35808</ExpertLink>
                                    <Name lang="en">Malignant sex cord stromal tumor of ovary</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="4">
                                    <ClassificationNode>
                                      <Disorder id="14487">
                                        <OrphaCode>99914</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99914</ExpertLink>
                                        <Name lang="en">Gynandroblastoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14488">
                                        <OrphaCode>99915</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99915</ExpertLink>
                                        <Name lang="en">Malignant granulosa cell tumor of the ovary</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14489">
                                        <OrphaCode>99916</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99916</ExpertLink>
                                        <Name lang="en">Malignant Sertoli-Leydig cell tumor of the ovary</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14490">
                                        <OrphaCode>99917</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99917</ExpertLink>
                                        <Name lang="en">Theca steroid-producing cell malignant tumor of ovary, not further specified</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18502">
                                    <OrphaCode>206484</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=206484</ExpertLink>
                                    <Name lang="en">Gonadoblastoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22495">
                                    <OrphaCode>370396</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370396</ExpertLink>
                                    <Name lang="en">Small cell carcinoma of the ovary</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="22744">
                                    <OrphaCode>398987</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398987</ExpertLink>
                                    <Name lang="en">Malignant teratoma of ovary</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32322">
                            <OrphaCode>696830</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=696830</ExpertLink>
                            <Name lang="en">Female adnexal tumor of probable Wolffian origin</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18134">
                        <OrphaCode>180250</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180250</ExpertLink>
                        <Name lang="en">Rare breast tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="18135">
                            <OrphaCode>180253</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180253</ExpertLink>
                            <Name lang="en">Rare benign breast tumor</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="18137">
                                <OrphaCode>180261</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180261</ExpertLink>
                                <Name lang="en">Phyllodes tumor of the breast</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18138">
                                <OrphaCode>180267</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180267</ExpertLink>
                                <Name lang="en">Giant adenofibroma of the breast</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18136">
                            <OrphaCode>180257</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180257</ExpertLink>
                            <Name lang="en">Rare malignant breast tumor</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="7">
                            <ClassificationNode>
                              <Disorder id="3384">
                                <OrphaCode>145</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=145</ExpertLink>
                                <Name lang="en">Hereditary breast and/or ovarian cancer syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18137">
                                <OrphaCode>180261</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180261</ExpertLink>
                                <Name lang="en">Phyllodes tumor of the breast</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18141">
                                <OrphaCode>180275</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180275</ExpertLink>
                                <Name lang="en">Paget disease of the nipple</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18746">
                                <OrphaCode>213528</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213528</ExpertLink>
                                <Name lang="en">Rare adenocarcinoma of the breast</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18747">
                                <OrphaCode>213531</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213531</ExpertLink>
                                <Name lang="en">Metaplastic carcinoma of the breast</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18748">
                                <OrphaCode>213557</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213557</ExpertLink>
                                <Name lang="en">Salivary gland type cancer of the breast</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32283">
                                <OrphaCode>694963</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=694963</ExpertLink>
                                <Name lang="en">Inflammatory breast cancer</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18149">
                        <OrphaCode>180312</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180312</ExpertLink>
                        <Name lang="en">Rare vulvovaginal tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="16678">
                            <OrphaCode>137583</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137583</ExpertLink>
                            <Name lang="en">Vulvar intraepithelial neoplasia</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18133">
                            <OrphaCode>180247</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=180247</ExpertLink>
                            <Name lang="en">Vaginal carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18503">
                            <OrphaCode>206489</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=206489</ExpertLink>
                            <Name lang="en">Malignant germ cell tumor of the vagina</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18504">
                            <OrphaCode>206492</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=206492</ExpertLink>
                            <Name lang="en">Vulvovaginal rhabdomyosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="25670">
                            <OrphaCode>494418</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494418</ExpertLink>
                            <Name lang="en">Vulvar carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="25677">
                                <OrphaCode>494448</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494448</ExpertLink>
                                <Name lang="en">Vulvar squamous cell carcinoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="25678">
                                <OrphaCode>494451</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494451</ExpertLink>
                                <Name lang="en">Vulvar basal cell carcinoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="25679">
                                <OrphaCode>494454</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494454</ExpertLink>
                                <Name lang="en">Vulvar adenocarcinoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18749">
                        <OrphaCode>213564</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213564</ExpertLink>
                        <Name lang="en">Rare uterine cancer</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="18750">
                            <OrphaCode>213569</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213569</ExpertLink>
                            <Name lang="en">Rare cancer of corpus uteri</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="10">
                            <ClassificationNode>
                              <Disorder id="18752">
                                <OrphaCode>213589</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213589</ExpertLink>
                                <Name lang="en">Malignant mixed epithelial and mesenchymal tumor of corpus uteri</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="18753">
                                    <OrphaCode>213600</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213600</ExpertLink>
                                    <Name lang="en">Adenosarcoma of the corpus uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18754">
                                    <OrphaCode>213605</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213605</ExpertLink>
                                    <Name lang="en">Carcinofibroma of the corpus uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18755">
                                    <OrphaCode>213610</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213610</ExpertLink>
                                    <Name lang="en">Carcinosarcoma of the corpus uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18757">
                                <OrphaCode>213620</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213620</ExpertLink>
                                <Name lang="en">Sarcoma of the corpus uteri</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="18756">
                                    <OrphaCode>213615</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213615</ExpertLink>
                                    <Name lang="en">Rhabdomyosarcoma of the corpus uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18758">
                                    <OrphaCode>213625</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213625</ExpertLink>
                                    <Name lang="en">Leiomyosarcoma of the corpus uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18759">
                                    <OrphaCode>213630</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213630</ExpertLink>
                                    <Name lang="en">Primitive neuroectodermal tumor of the corpus uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18760">
                                <OrphaCode>213711</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213711</ExpertLink>
                                <Name lang="en">Endometrial stromal sarcoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18761">
                                <OrphaCode>213716</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213716</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18762">
                                <OrphaCode>213721</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213721</ExpertLink>
                                <Name lang="en">Undifferentiated carcinoma of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18763">
                                <OrphaCode>213726</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213726</ExpertLink>
                                <Name lang="en">Serous carcinoma of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18764">
                                <OrphaCode>213731</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213731</ExpertLink>
                                <Name lang="en">High-grade neuroendocrine carcinoma of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18765">
                                <OrphaCode>213736</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213736</ExpertLink>
                                <Name lang="en">Low-grade neuroendocrine tumor of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18767">
                                <OrphaCode>213746</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213746</ExpertLink>
                                <Name lang="en">Transitional cell carcinoma of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18768">
                                <OrphaCode>213751</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213751</ExpertLink>
                                <Name lang="en">Malignant germ cell tumor of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18769">
                            <OrphaCode>213761</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213761</ExpertLink>
                            <Name lang="en">Rare cancer of cervix uteri</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="9">
                            <ClassificationNode>
                              <Disorder id="18770">
                                <OrphaCode>213767</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213767</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18771">
                                <OrphaCode>213772</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213772</ExpertLink>
                                <Name lang="en">Adenocarcinoma of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18772">
                                <OrphaCode>213777</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213777</ExpertLink>
                                <Name lang="en">High-grade neuroendocrine carcinoma of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18773">
                                <OrphaCode>213782</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213782</ExpertLink>
                                <Name lang="en">Malignant mixed epithelial and mesenchymal tumor of cervix uteri</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="18774">
                                    <OrphaCode>213787</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213787</ExpertLink>
                                    <Name lang="en">Carcinosarcoma of the cervix uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18775">
                                    <OrphaCode>213792</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213792</ExpertLink>
                                    <Name lang="en">Adenosarcoma of the cervix uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18776">
                                <OrphaCode>213797</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213797</ExpertLink>
                                <Name lang="en">Sarcoma of cervix uteri</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="18777">
                                    <OrphaCode>213802</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213802</ExpertLink>
                                    <Name lang="en">Rhabdomyosarcoma of the cervix uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18778">
                                    <OrphaCode>213807</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213807</ExpertLink>
                                    <Name lang="en">Leiomyosarcoma of the cervix uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18779">
                                    <OrphaCode>213812</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213812</ExpertLink>
                                    <Name lang="en">Primitive neuroectodermal tumor of the cervix uteri</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18781">
                                <OrphaCode>213823</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213823</ExpertLink>
                                <Name lang="en">Adenoid cystic carcinoma of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18782">
                                <OrphaCode>213828</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213828</ExpertLink>
                                <Name lang="en">Adenoid basal carcinoma of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18783">
                                <OrphaCode>213833</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213833</ExpertLink>
                                <Name lang="en">Glassy cell carcinoma of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18784">
                                <OrphaCode>213837</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213837</ExpertLink>
                                <Name lang="en">Malignant germ cell tumor of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19762">
                        <OrphaCode>254685</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=254685</ExpertLink>
                        <Name lang="en">Gestational trophoblastic disease</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="10790">
                            <OrphaCode>59305</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=59305</ExpertLink>
                            <Name lang="en">Gestational trophoblastic neoplasm</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="14498">
                                <OrphaCode>99925</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99925</ExpertLink>
                                <Name lang="en">Invasive mole</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14499">
                                <OrphaCode>99926</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99926</ExpertLink>
                                <Name lang="en">Gestational choriocarcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14501">
                                <OrphaCode>99928</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99928</ExpertLink>
                                <Name lang="en">Placental site trophoblastic tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19765">
                                <OrphaCode>254698</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=254698</ExpertLink>
                                <Name lang="en">Epithelioid trophoblastic tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14500">
                            <OrphaCode>99927</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99927</ExpertLink>
                            <Name lang="en">Hydatidiform mole</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="19763">
                                <OrphaCode>254688</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=254688</ExpertLink>
                                <Name lang="en">Complete hydatidiform mole</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="19764">
                                <OrphaCode>254693</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=254693</ExpertLink>
                                <Name lang="en">Partial hydatidiform mole</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="14668">
                    <OrphaCode>100100</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100100</ExpertLink>
                    <Name lang="en">Thymic tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="2">
                    <ClassificationNode>
                      <Disorder id="3764">
                        <OrphaCode>3398</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3398</ExpertLink>
                        <Name lang="en">Thymic epithelial neoplasm</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="14440">
                            <OrphaCode>99867</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99867</ExpertLink>
                            <Name lang="en">Thymoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="20040">
                                <OrphaCode>263310</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263310</ExpertLink>
                                <Name lang="en">Thymoma type A</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20041">
                                <OrphaCode>263317</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263317</ExpertLink>
                                <Name lang="en">Thymoma type B</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20042">
                                <OrphaCode>263324</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263324</ExpertLink>
                                <Name lang="en">Thymoma type AB</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14441">
                            <OrphaCode>99868</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99868</ExpertLink>
                            <Name lang="en">Thymic carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14442">
                            <OrphaCode>99869</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99869</ExpertLink>
                            <Name lang="en">Thymic neuroendocrine carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="20043">
                                <OrphaCode>263331</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263331</ExpertLink>
                                <Name lang="en">Well-differentiated thymic neuroendocrine carcinoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20044">
                                <OrphaCode>263335</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263335</ExpertLink>
                                <Name lang="en">Moderately-differentiated thymic neuroendocrine carcinoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20045">
                                <OrphaCode>263339</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263339</ExpertLink>
                                <Name lang="en">Poorly differentiated thymic neuroendocrine carcinoma</Name>
                                <DisorderType id="21457">
                                  <Name lang="en">Histopathological subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12882">
                        <OrphaCode>97289</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97289</ExpertLink>
                        <Name lang="en">Thymic neuroendocrine tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="14886">
                    <OrphaCode>101950</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101950</ExpertLink>
                    <Name lang="en">Rare eye tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="15">
                    <ClassificationNode>
                      <Disorder id="122">
                        <OrphaCode>790</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=790</ExpertLink>
                        <Name lang="en">Retinoblastoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="22197">
                            <OrphaCode>357027</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=357027</ExpertLink>
                            <Name lang="en">Hereditary retinoblastoma</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22198">
                            <OrphaCode>357034</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=357034</ExpertLink>
                            <Name lang="en">Non-hereditary retinoblastoma</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="185">
                        <OrphaCode>636</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=636</ExpertLink>
                        <Name lang="en">Neurofibromatosis type 1</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="12945">
                            <OrphaCode>97685</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97685</ExpertLink>
                            <Name lang="en">17q11 microdeletion syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22341">
                            <OrphaCode>363700</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363700</ExpertLink>
                            <Name lang="en">Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10714">
                        <OrphaCode>52994</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=52994</ExpertLink>
                        <Name lang="en">Orbital leiomyoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12147">
                        <OrphaCode>91481</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91481</ExpertLink>
                        <Name lang="en">Ring dermoid of cornea</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20167">
                        <OrphaCode>268139</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=268139</ExpertLink>
                        <Name lang="en">Intraocular medulloepithelioma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20411">
                        <OrphaCode>279897</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=279897</ExpertLink>
                        <Name lang="en">Primary oculocerebral lymphoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22142">
                        <OrphaCode>353356</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=353356</ExpertLink>
                        <Name lang="en">Vasoproliferative tumor of the retina</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23414">
                        <OrphaCode>440727</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=440727</ExpertLink>
                        <Name lang="en">Combined hamartoma of the retina and retinal pigment epithelium</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31370">
                        <OrphaCode>617910</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=617910</ExpertLink>
                        <Name lang="en">Conjunctival malignant melanoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31939">
                        <OrphaCode>658590</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=658590</ExpertLink>
                        <Name lang="en">Eyelid sebaceous carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31972">
                        <OrphaCode>659744</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=659744</ExpertLink>
                        <Name lang="en">Ocular surface squamous neoplasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32643">
                        <OrphaCode>716198</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=716198</ExpertLink>
                        <Name lang="en">Rare paraneoplastic choroidal disorder</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="1">
                        <ClassificationNode>
                          <Disorder id="32104">
                            <OrphaCode>674968</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=674968</ExpertLink>
                            <Name lang="en">Bilateral diffuse uveal melanocytic proliferation disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32645">
                        <OrphaCode>716204</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=716204</ExpertLink>
                        <Name lang="en">Rare neoplastic choroidal disorder</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="32646">
                            <OrphaCode>716207</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=716207</ExpertLink>
                            <Name lang="en">Rare benign neoplastic choroidal disorder</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="1">
                            <ClassificationNode>
                              <Disorder id="32103">
                                <OrphaCode>674965</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=674965</ExpertLink>
                                <Name lang="en">Choroidal osteoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32647">
                            <OrphaCode>716210</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=716210</ExpertLink>
                            <Name lang="en">Rare malignant neoplastic choroidal disorder</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="32545">
                                <OrphaCode>714046</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714046</ExpertLink>
                                <Name lang="en">Primary choroidal lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32825">
                                <OrphaCode>723203</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=723203</ExpertLink>
                                <Name lang="en">Choroidal and ciliary body melanoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32637">
                        <OrphaCode>715862</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715862</ExpertLink>
                        <Name lang="en">Melanocytoma of the optic disc and optic nerve</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32824">
                        <OrphaCode>723195</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=723195</ExpertLink>
                        <Name lang="en">Iris melanoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="17740">
                    <OrphaCode>168194</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168194</ExpertLink>
                    <Name lang="en">Rare cardiac tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="6">
                    <ClassificationNode>
                      <Disorder id="2389">
                        <OrphaCode>1359</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1359</ExpertLink>
                        <Name lang="en">Carney complex</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8593">
                        <OrphaCode>615</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=615</ExpertLink>
                        <Name lang="en">Familial atrial myxoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8594">
                        <OrphaCode>874</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=874</ExpertLink>
                        <Name lang="en">Primary adult heart tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8607">
                        <OrphaCode>875</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=875</ExpertLink>
                        <Name lang="en">Primary pediatric heart tumor</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21650">
                        <OrphaCode>319340</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319340</ExpertLink>
                        <Name lang="en">Carney complex-trismus-pseudocamptodactyly syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32162">
                        <OrphaCode>685004</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=685004</ExpertLink>
                        <Name lang="en">Primary pericardial mesothelioma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="17794">
                    <OrphaCode>168803</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168803</ExpertLink>
                    <Name lang="en">Primary peritoneal tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="2">
                    <ClassificationNode>
                      <Disorder id="17795">
                        <OrphaCode>168807</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168807</ExpertLink>
                        <Name lang="en">Primary malignant peritoneal tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="8765">
                            <OrphaCode>26790</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=26790</ExpertLink>
                            <Name lang="en">Pseudomyxoma peritonei</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11579">
                            <OrphaCode>83469</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=83469</ExpertLink>
                            <Name lang="en">Desmoplastic small round cell tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17796">
                            <OrphaCode>168811</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168811</ExpertLink>
                            <Name lang="en">Malignant peritoneal mesothelioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17798">
                            <OrphaCode>168829</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168829</ExpertLink>
                            <Name lang="en">Primary peritoneal carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32139">
                            <OrphaCode>676036</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=676036</ExpertLink>
                            <Name lang="en">Peritoneal mesothelioma in situ</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32137">
                        <OrphaCode>676030</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=676030</ExpertLink>
                        <Name lang="en">Primary benign peritoneal tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="4">
                        <ClassificationNode>
                          <Disorder id="10996">
                            <OrphaCode>71274</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=71274</ExpertLink>
                            <Name lang="en">Disseminated peritoneal leiomyomatosis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17797">
                            <OrphaCode>168816</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168816</ExpertLink>
                            <Name lang="en">Peritoneal inclusion cyst</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32136">
                            <OrphaCode>675976</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675976</ExpertLink>
                            <Name lang="en">Adenomatoid tumor of the peritoneum</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32138">
                            <OrphaCode>676033</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=676033</ExpertLink>
                            <Name lang="en">Well-differentiated papillary mesothelial tumor of the peritoneum</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18217">
                    <OrphaCode>182114</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182114</ExpertLink>
                    <Name lang="en">Rare urogenital tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="3">
                    <ClassificationNode>
                      <Disorder id="13076">
                        <OrphaCode>98058</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98058</ExpertLink>
                        <Name lang="en">Rare urinary tract tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="20605">
                            <OrphaCode>284400</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=284400</ExpertLink>
                            <Name lang="en">Small cell carcinoma of the bladder</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="25898">
                            <OrphaCode>498228</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=498228</ExpertLink>
                            <Name lang="en">Phyllodes tumor of the prostate</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="29876">
                            <OrphaCode>598216</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=598216</ExpertLink>
                            <Name lang="en">Upper tract urothelial carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32287">
                            <OrphaCode>695020</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=695020</ExpertLink>
                            <Name lang="en">Urachal carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32288">
                            <OrphaCode>695023</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=695023</ExpertLink>
                            <Name lang="en">Pure squamous carcinoma of the urothelial tract</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22308">
                        <OrphaCode>363472</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363472</ExpertLink>
                        <Name lang="en">Tumor of testis and paratestis</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="18502">
                            <OrphaCode>206484</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=206484</ExpertLink>
                            <Name lang="en">Gonadoblastoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22309">
                            <OrphaCode>363478</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363478</ExpertLink>
                            <Name lang="en">Paratesticular adenocarcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22310">
                            <OrphaCode>363483</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363483</ExpertLink>
                            <Name lang="en">Testicular teratoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22311">
                            <OrphaCode>363489</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363489</ExpertLink>
                            <Name lang="en">Sex cord-stromal tumor of testis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22313">
                            <OrphaCode>363504</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363504</ExpertLink>
                            <Name lang="en">Germ cell tumor of testis</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="3762">
                                <OrphaCode>842</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=842</ExpertLink>
                                <Name lang="en">Testicular seminomatous germ cell tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14438">
                                <OrphaCode>99865</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99865</ExpertLink>
                                <Name lang="en">Spermatocytic seminoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22312">
                                <OrphaCode>363494</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363494</ExpertLink>
                                <Name lang="en">Non-seminomatous germ cell tumor of testis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32163">
                            <OrphaCode>685010</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=685010</ExpertLink>
                            <Name lang="en">Mesothelioma of the tunica vaginalis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22716">
                        <OrphaCode>398043</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398043</ExpertLink>
                        <Name lang="en">Malignant tumor of penis</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="22717">
                            <OrphaCode>398053</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398053</ExpertLink>
                            <Name lang="en">Adenocarcinoma of the penis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22718">
                            <OrphaCode>398058</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398058</ExpertLink>
                            <Name lang="en">Squamous cell carcinoma of the penis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18222">
                    <OrphaCode>182130</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=182130</ExpertLink>
                    <Name lang="en">Tumor of endocrine glands</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="7">
                    <ClassificationNode>
                      <Disorder id="8685">
                        <OrphaCode>877</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=877</ExpertLink>
                        <Name lang="en">Neuroendocrine neoplasm</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="14664">
                            <OrphaCode>100092</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100092</ExpertLink>
                            <Name lang="en">Gastroenteropancreatic neuroendocrine neoplasm</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="25237">
                                <OrphaCode>481508</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=481508</ExpertLink>
                                <Name lang="en">Gastroenteric neuroendocrine neoplasm</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="7">
                                <ClassificationNode>
                                  <Disorder id="14647">
                                    <OrphaCode>100075</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100075</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of stomach</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14651">
                                    <OrphaCode>100079</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100079</ExpertLink>
                                    <Name lang="en">Neuroendocrine neoplasm of appendix</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="21952">
                                        <OrphaCode>329977</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=329977</ExpertLink>
                                        <Name lang="en">Classic neuroendocrine tumor of appendix</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="21953">
                                        <OrphaCode>329984</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=329984</ExpertLink>
                                        <Name lang="en">Goblet cell carcinoma</Name>
                                        <DisorderType id="21450">
                                          <Name lang="en">Clinical subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14652">
                                    <OrphaCode>100080</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100080</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of the colon</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14653">
                                    <OrphaCode>100081</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100081</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of the rectum</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14654">
                                    <OrphaCode>100082</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100082</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of anal canal</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23177">
                                    <OrphaCode>423975</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=423975</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of the small intestine</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="3">
                                    <ClassificationNode>
                                      <Disorder id="14648">
                                        <OrphaCode>100076</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100076</ExpertLink>
                                        <Name lang="en">Duodenal neuroendocrine tumor</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="2">
                                        <ClassificationNode>
                                          <Disorder id="3595">
                                            <OrphaCode>913</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=913</ExpertLink>
                                            <Name lang="en">Zollinger-Ellison syndrome</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12878">
                                            <OrphaCode>97283</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97283</ExpertLink>
                                            <Name lang="en">Somatostatinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14649">
                                        <OrphaCode>100077</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100077</ExpertLink>
                                        <Name lang="en">Jejunal neuroendocrine tumor</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="1">
                                        <ClassificationNode>
                                          <Disorder id="12878">
                                            <OrphaCode>97283</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97283</ExpertLink>
                                            <Name lang="en">Somatostatinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14650">
                                        <OrphaCode>100078</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100078</ExpertLink>
                                        <Name lang="en">Ileal neuroendocrine tumor</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="26440">
                                    <OrphaCode>506136</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506136</ExpertLink>
                                    <Name lang="en">Neuroendocrine neoplasm of esophagus</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="26433">
                                <OrphaCode>506052</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506052</ExpertLink>
                                <Name lang="en">Neuroendocrine neoplasm of pancreas</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="12870">
                                    <OrphaCode>97253</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97253</ExpertLink>
                                    <Name lang="en">Neuroendocrine tumor of pancreas</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="26434">
                                        <OrphaCode>506060</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506060</ExpertLink>
                                        <Name lang="en">Functioning neuroendocrine tumor of pancreas</Name>
                                        <DisorderType id="36561">
                                          <Name lang="en">Category</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="9">
                                        <ClassificationNode>
                                          <Disorder id="3595">
                                            <OrphaCode>913</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=913</ExpertLink>
                                            <Name lang="en">Zollinger-Ellison syndrome</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12871">
                                            <OrphaCode>97261</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97261</ExpertLink>
                                            <Name lang="en">GRFoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12874">
                                            <OrphaCode>97278</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97278</ExpertLink>
                                            <Name lang="en">PPoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12875">
                                            <OrphaCode>97279</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97279</ExpertLink>
                                            <Name lang="en">Insulinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12876">
                                            <OrphaCode>97280</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97280</ExpertLink>
                                            <Name lang="en">Glucagonoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12877">
                                            <OrphaCode>97282</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97282</ExpertLink>
                                            <Name lang="en">VIPoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="12878">
                                            <OrphaCode>97283</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97283</ExpertLink>
                                            <Name lang="en">Somatostatinoma</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="14462">
                                            <OrphaCode>99889</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99889</ExpertLink>
                                            <Name lang="en">Cushing syndrome due to ectopic ACTH secretion</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                        <ClassificationNode>
                                          <Disorder id="26436">
                                            <OrphaCode>506090</OrphaCode>
                                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506090</ExpertLink>
                                            <Name lang="en">Serotonin-producing neuroendocrine tumor of pancreas</Name>
                                            <DisorderType id="21394">
                                              <Name lang="en">Disease</Name>
                                            </DisorderType>
                                          </Disorder>
                                          <ClassificationNodeChildList count="0">
                                          </ClassificationNodeChildList>
                                        </ClassificationNode>
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="26435">
                                        <OrphaCode>506075</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506075</ExpertLink>
                                        <Name lang="en">Non-functioning neuroendocrine tumor of pancreas</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="26437">
                                    <OrphaCode>506098</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506098</ExpertLink>
                                    <Name lang="en">Neuroendocrine carcinoma of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="26438">
                                    <OrphaCode>506112</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=506112</ExpertLink>
                                    <Name lang="en">Mixed neuroendocrine and non-neuroendocrine neoplasm of pancreas</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14665">
                            <OrphaCode>100093</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100093</ExpertLink>
                            <Name lang="en">Carcinoid syndrome</Name>
                            <DisorderType id="21422">
                              <Name lang="en">Clinical syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14669">
                            <OrphaCode>100101</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100101</ExpertLink>
                            <Name lang="en">Neuroendocrine tumor with other location</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="12">
                            <ClassificationNode>
                              <Disorder id="6023">
                                <OrphaCode>178</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=178</ExpertLink>
                                <Name lang="en">Chordoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11166">
                                <OrphaCode>79140</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79140</ExpertLink>
                                <Name lang="en">Cutaneous neuroendocrine carcinoma</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="12882">
                                <OrphaCode>97289</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97289</ExpertLink>
                                <Name lang="en">Thymic neuroendocrine tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14442">
                                <OrphaCode>99869</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99869</ExpertLink>
                                <Name lang="en">Thymic neuroendocrine carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="20043">
                                    <OrphaCode>263331</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263331</ExpertLink>
                                    <Name lang="en">Well-differentiated thymic neuroendocrine carcinoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20044">
                                    <OrphaCode>263335</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263335</ExpertLink>
                                    <Name lang="en">Moderately-differentiated thymic neuroendocrine carcinoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="20045">
                                    <OrphaCode>263339</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263339</ExpertLink>
                                    <Name lang="en">Poorly differentiated thymic neuroendocrine carcinoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14655">
                                <OrphaCode>100083</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100083</ExpertLink>
                                <Name lang="en">Laryngeal neuroendocrine tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14656">
                                <OrphaCode>100084</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100084</ExpertLink>
                                <Name lang="en">Middle ear neuroendocrine tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14657">
                                <OrphaCode>100085</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100085</ExpertLink>
                                <Name lang="en">Primary hepatic neuroendocrine carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14658">
                                <OrphaCode>100086</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100086</ExpertLink>
                                <Name lang="en">Gallbladder neuroendocrine tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18764">
                                <OrphaCode>213731</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213731</ExpertLink>
                                <Name lang="en">High-grade neuroendocrine carcinoma of the corpus uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="18772">
                                <OrphaCode>213777</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=213777</ExpertLink>
                                <Name lang="en">High-grade neuroendocrine carcinoma of the cervix uteri</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20605">
                                <OrphaCode>284400</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=284400</ExpertLink>
                                <Name lang="en">Small cell carcinoma of the bladder</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10741">
                        <OrphaCode>53715</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=53715</ExpertLink>
                        <Name lang="en">Familial tumoral calcinosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="21245">
                            <OrphaCode>306658</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306658</ExpertLink>
                            <Name lang="en">Familial normophosphatemic tumoral calcinosis</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21246">
                            <OrphaCode>306661</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306661</ExpertLink>
                            <Name lang="en">Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14659">
                        <OrphaCode>100087</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100087</ExpertLink>
                        <Name lang="en">Rare thyroid tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="12879">
                            <OrphaCode>97285</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97285</ExpertLink>
                            <Name lang="en">Thyroid lymphoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14660">
                            <OrphaCode>100088</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100088</ExpertLink>
                            <Name lang="en">Rare thyroid carcinoma</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="6">
                            <ClassificationNode>
                              <Disorder id="905">
                                <OrphaCode>146</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=146</ExpertLink>
                                <Name lang="en">Differentiated thyroid carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="906">
                                <OrphaCode>653</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=653</ExpertLink>
                                <Name lang="en">Multiple endocrine neoplasia type 2</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="19538">
                                    <OrphaCode>247698</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247698</ExpertLink>
                                    <Name lang="en">Multiple endocrine neoplasia type 2A</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19539">
                                    <OrphaCode>247709</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247709</ExpertLink>
                                    <Name lang="en">Multiple endocrine neoplasia type 2B</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8676">
                                <OrphaCode>142</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=142</ExpertLink>
                                <Name lang="en">Anaplastic thyroid carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8686">
                                <OrphaCode>1332</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1332</ExpertLink>
                                <Name lang="en">Medullary thyroid carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14205">
                                <OrphaCode>99361</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99361</ExpertLink>
                                <Name lang="en">Isolated familial medullary thyroid carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21662">
                                <OrphaCode>319494</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319494</ExpertLink>
                                <Name lang="en">Familial nonmedullary thyroid carcinoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="12883">
                                    <OrphaCode>97290</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97290</ExpertLink>
                                    <Name lang="en">Familial papillary thyroid carcinoma with renal papillary neoplasia</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21661">
                                    <OrphaCode>319487</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319487</ExpertLink>
                                    <Name lang="en">Familial papillary or follicular thyroid carcinoma</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="14662">
                        <OrphaCode>100090</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100090</ExpertLink>
                        <Name lang="en">Rare parathyroid tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="5545">
                            <OrphaCode>2207</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2207</ExpertLink>
                            <Name lang="en">Familial primary hyperparathyroidism</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="121">
                                <OrphaCode>652</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652</ExpertLink>
                                <Name lang="en">Multiple endocrine neoplasia type 1</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14452">
                                <OrphaCode>99879</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99879</ExpertLink>
                                <Name lang="en">Familial isolated hyperparathyroidism</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14453">
                                <OrphaCode>99880</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99880</ExpertLink>
                                <Name lang="en">Hyperparathyroidism-jaw tumor syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="8675">
                            <OrphaCode>143</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=143</ExpertLink>
                            <Name lang="en">Parathyroid carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14663">
                        <OrphaCode>100091</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100091</ExpertLink>
                        <Name lang="en">Adrenal/paraganglial tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="10">
                        <ClassificationNode>
                          <Disorder id="99">
                            <OrphaCode>892</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=892</ExpertLink>
                            <Name lang="en">Von Hippel-Lindau disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="121">
                            <OrphaCode>652</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652</ExpertLink>
                            <Name lang="en">Multiple endocrine neoplasia type 1</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2389">
                            <OrphaCode>1359</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1359</ExpertLink>
                            <Name lang="en">Carney complex</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3731">
                            <OrphaCode>1501</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1501</ExpertLink>
                            <Name lang="en">Adrenocortical carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="8738">
                            <OrphaCode>404</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404</ExpertLink>
                            <Name lang="en">Familial hyperaldosteronism type II</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12125">
                            <OrphaCode>91351</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91351</ExpertLink>
                            <Name lang="en">Pituitary dermoid and epidermoid cysts</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19538">
                            <OrphaCode>247698</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247698</ExpertLink>
                            <Name lang="en">Multiple endocrine neoplasia type 2A</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19539">
                            <OrphaCode>247709</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247709</ExpertLink>
                            <Name lang="en">Multiple endocrine neoplasia type 2B</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="28814">
                            <OrphaCode>573163</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=573163</ExpertLink>
                            <Name lang="en">Pheochromocytoma-paraganglioma</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="8775">
                                <OrphaCode>29072</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=29072</ExpertLink>
                                <Name lang="en">Hereditary pheochromocytoma-paraganglioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="12552">
                                <OrphaCode>94080</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=94080</ExpertLink>
                                <Name lang="en">Non-functioning paraganglioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20390">
                                <OrphaCode>276621</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276621</ExpertLink>
                                <Name lang="en">Sporadic pheochromocytoma/secreting paraganglioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21762">
                                <OrphaCode>324299</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=324299</ExpertLink>
                                <Name lang="en">EPAS1-related polycythemia-pheochromocytoma/paraganglioma syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="31860">
                            <OrphaCode>649017</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=649017</ExpertLink>
                            <Name lang="en">Rare adrenocortical nodular disease</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="31811">
                                <OrphaCode>647772</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=647772</ExpertLink>
                                <Name lang="en">Isolated primary pigmented nodular adrenocortical disease</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="31812">
                                <OrphaCode>647782</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=647782</ExpertLink>
                                <Name lang="en">Isolated micronodular adrenocortical disease</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14666">
                        <OrphaCode>100094</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100094</ExpertLink>
                        <Name lang="en">Multiple polyglandular tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="99">
                            <OrphaCode>892</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=892</ExpertLink>
                            <Name lang="en">Von Hippel-Lindau disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2389">
                            <OrphaCode>1359</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1359</ExpertLink>
                            <Name lang="en">Carney complex</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12880">
                            <OrphaCode>97286</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97286</ExpertLink>
                            <Name lang="en">Carney-Stratakis syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="16888">
                            <OrphaCode>139411</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=139411</ExpertLink>
                            <Name lang="en">Carney triad</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20351">
                            <OrphaCode>276161</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276161</ExpertLink>
                            <Name lang="en">Multiple endocrine neoplasia</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="121">
                                <OrphaCode>652</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652</ExpertLink>
                                <Name lang="en">Multiple endocrine neoplasia type 1</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="906">
                                <OrphaCode>653</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=653</ExpertLink>
                                <Name lang="en">Multiple endocrine neoplasia type 2</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="19538">
                                    <OrphaCode>247698</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247698</ExpertLink>
                                    <Name lang="en">Multiple endocrine neoplasia type 2A</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="19539">
                                    <OrphaCode>247709</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247709</ExpertLink>
                                    <Name lang="en">Multiple endocrine neoplasia type 2B</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20350">
                                <OrphaCode>276152</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276152</ExpertLink>
                                <Name lang="en">Multiple endocrine neoplasia type 4</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21184">
                        <OrphaCode>304055</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=304055</ExpertLink>
                        <Name lang="en">Pituitary tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="14209">
                            <OrphaCode>99408</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99408</ExpertLink>
                            <Name lang="en">Pituitary adenoma</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="12123">
                                <OrphaCode>91349</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91349</ExpertLink>
                                <Name lang="en">Non-functioning pituitary adenoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="21529">
                                    <OrphaCode>314786</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314786</ExpertLink>
                                    <Name lang="en">Silent pituitary adenoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21530">
                                    <OrphaCode>314790</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314790</ExpertLink>
                                    <Name lang="en">Null pituitary adenoma</Name>
                                    <DisorderType id="21457">
                                      <Name lang="en">Histopathological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21524">
                                <OrphaCode>314753</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314753</ExpertLink>
                                <Name lang="en">Functioning pituitary adenoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="7">
                                <ClassificationNode>
                                  <Disorder id="3387">
                                    <OrphaCode>2965</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2965</ExpertLink>
                                    <Name lang="en">Prolactinoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12121">
                                    <OrphaCode>91347</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91347</ExpertLink>
                                    <Name lang="en">TSH-secreting pituitary adenoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12122">
                                    <OrphaCode>91348</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91348</ExpertLink>
                                    <Name lang="en">Functioning gonadotropic adenoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12827">
                                    <OrphaCode>96253</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96253</ExpertLink>
                                    <Name lang="en">Cushing disease</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12829">
                                    <OrphaCode>96256</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96256</ExpertLink>
                                    <Name lang="en">Somatotropic adenoma</Name>
                                    <DisorderType id="21436">
                                      <Name lang="en">Clinical group</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="2">
                                    <ClassificationNode>
                                      <Disorder id="408">
                                        <OrphaCode>963</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=963</ExpertLink>
                                        <Name lang="en">Acromegaly</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="14298">
                                        <OrphaCode>99725</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99725</ExpertLink>
                                        <Name lang="en">Pituitary gigantism</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="18380">
                                    <OrphaCode>199244</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=199244</ExpertLink>
                                    <Name lang="en">Nelson syndrome</Name>
                                    <DisorderType id="21422">
                                      <Name lang="en">Clinical syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="21525">
                                    <OrphaCode>314759</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314759</ExpertLink>
                                    <Name lang="en">Mixed functioning pituitary adenoma</Name>
                                    <DisorderType id="36561">
                                      <Name lang="en">Category</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="1">
                                    <ClassificationNode>
                                      <Disorder id="21527">
                                        <OrphaCode>314769</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314769</ExpertLink>
                                        <Name lang="en">Somatomammotropinoma</Name>
                                        <DisorderType id="21394">
                                          <Name lang="en">Disease</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21528">
                                <OrphaCode>314777</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314777</ExpertLink>
                                <Name lang="en">Familial isolated pituitary adenoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21118">
                            <OrphaCode>300385</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300385</ExpertLink>
                            <Name lang="en">Pituitary carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18710">
                    <OrphaCode>211237</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211237</ExpertLink>
                    <Name lang="en">Rare vascular tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="3">
                    <ClassificationNode>
                      <Disorder id="32077">
                        <OrphaCode>673466</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673466</ExpertLink>
                        <Name lang="en">Malignant vascular tumor</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="17144">
                            <OrphaCode>157791</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=157791</ExpertLink>
                            <Name lang="en">Epithelioid hemangioendothelioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20050">
                            <OrphaCode>263413</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=263413</ExpertLink>
                            <Name lang="en">Angiosarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32078">
                        <OrphaCode>673470</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673470</ExpertLink>
                        <Name lang="en">Benign vascular tumor</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="20">
                        <ClassificationNode>
                          <Disorder id="32576">
                            <OrphaCode>714692</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714692</ExpertLink>
                            <Name lang="en">Congenital disseminated pyogenic granuloma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32832">
                            <OrphaCode>723270</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=723270</ExpertLink>
                            <Name lang="en">Isolated glomeruloid hemangioma</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32833">
                            <OrphaCode>723286</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=723286</ExpertLink>
                            <Name lang="en">Cutaneous epithelioid angiomatous nodule</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="1359">
                            <OrphaCode>1062</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1062</ExpertLink>
                            <Name lang="en">Hereditary neurocutaneous malformation</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3543">
                            <OrphaCode>1063</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1063</ExpertLink>
                            <Name lang="en">Tufted angioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10988">
                            <OrphaCode>71213</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=71213</ExpertLink>
                            <Name lang="en">Retinal cavernous hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18698">
                            <OrphaCode>210584</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=210584</ExpertLink>
                            <Name lang="en">Spindle cell hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18699">
                            <OrphaCode>210589</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=210589</ExpertLink>
                            <Name lang="en">Rare infantile hemangioma</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="5">
                            <ClassificationNode>
                              <Disorder id="32110">
                                <OrphaCode>675380</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675380</ExpertLink>
                                <Name lang="en">Isolated segmental infantile hemangioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="2030">
                                <OrphaCode>2123</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2123</ExpertLink>
                                <Name lang="en">Multifocal infantile hemangioma with extracutenous involvement</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10577">
                                <OrphaCode>42775</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=42775</ExpertLink>
                                <Name lang="en">PHACE syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11599">
                                <OrphaCode>83628</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=83628</ExpertLink>
                                <Name lang="en">LUMBAR syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="16751">
                                <OrphaCode>137935</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137935</ExpertLink>
                                <Name lang="en">Airway infantile hemangioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23753">
                            <OrphaCode>458775</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458775</ExpertLink>
                            <Name lang="en">Congenital hemangioma</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="17055">
                                <OrphaCode>141179</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141179</ExpertLink>
                                <Name lang="en">Non-involuting congenital hemangioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17056">
                                <OrphaCode>141184</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141184</ExpertLink>
                                <Name lang="en">Rapidly involuting congenital hemangioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23754">
                                <OrphaCode>458785</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458785</ExpertLink>
                                <Name lang="en">Partially involuting congenital hemangioma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32080">
                            <OrphaCode>673525</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673525</ExpertLink>
                            <Name lang="en">Intravascular papillary endothelial hyperplasia</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32081">
                            <OrphaCode>673538</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673538</ExpertLink>
                            <Name lang="en">Littoral cell hemangioma of the spleen</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32082">
                            <OrphaCode>673543</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673543</ExpertLink>
                            <Name lang="en">Papillary hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32086">
                            <OrphaCode>673568</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673568</ExpertLink>
                            <Name lang="en">Eccrine angiomatous hamartoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32087">
                            <OrphaCode>673574</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673574</ExpertLink>
                            <Name lang="en">Reactive angioendotheliomatosis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32106">
                            <OrphaCode>675359</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675359</ExpertLink>
                            <Name lang="en">Anastomosing hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32107">
                            <OrphaCode>675362</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675362</ExpertLink>
                            <Name lang="en">Hobnail hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32108">
                            <OrphaCode>675369</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675369</ExpertLink>
                            <Name lang="en">Microvenular hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32112">
                            <OrphaCode>675396</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675396</ExpertLink>
                            <Name lang="en">Epithelioid hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32115">
                            <OrphaCode>675597</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=675597</ExpertLink>
                            <Name lang="en">Acquired elastotic hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32552">
                            <OrphaCode>714138</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714138</ExpertLink>
                            <Name lang="en">Circumscribed choroidal hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32079">
                        <OrphaCode>673473</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673473</ExpertLink>
                        <Name lang="en">Borderline vascular tumor</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="7">
                        <ClassificationNode>
                          <Disorder id="24018">
                            <OrphaCode>464321</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=464321</ExpertLink>
                            <Name lang="en">Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3544">
                            <OrphaCode>2122</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2122</ExpertLink>
                            <Name lang="en">Kaposiform hemangioendothelioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10316">
                            <OrphaCode>33276</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33276</ExpertLink>
                            <Name lang="en">Kaposi sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23750">
                            <OrphaCode>458758</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458758</ExpertLink>
                            <Name lang="en">Composite hemangioendothelioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23751">
                            <OrphaCode>458763</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458763</ExpertLink>
                            <Name lang="en">Retiform hemangioendothelioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23752">
                            <OrphaCode>458768</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458768</ExpertLink>
                            <Name lang="en">Papillary intralymphatic angioendothelioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32085">
                            <OrphaCode>673556</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=673556</ExpertLink>
                            <Name lang="en">Pseudomyogenic hemangioendothelioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="20751">
                    <OrphaCode>289635</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289635</ExpertLink>
                    <Name lang="en">Rare virus associated tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="5">
                    <ClassificationNode>
                      <Disorder id="11166">
                        <OrphaCode>79140</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79140</ExpertLink>
                        <Name lang="en">Cutaneous neuroendocrine carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="11768">
                        <OrphaCode>86875</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86875</ExpertLink>
                        <Name lang="en">Adult T-cell leukemia/lymphoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14960">
                        <OrphaCode>102024</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=102024</ExpertLink>
                        <Name lang="en">Human herpesvirus 8-related disorder</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="10316">
                            <OrphaCode>33276</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33276</ExpertLink>
                            <Name lang="en">Kaposi sarcoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10631">
                            <OrphaCode>48686</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=48686</ExpertLink>
                            <Name lang="en">Primary effusion lymphoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="28675">
                            <OrphaCode>570438</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=570438</ExpertLink>
                            <Name lang="en">HHV-8-associated multicentric Castleman disease</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20752">
                        <OrphaCode>289638</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289638</ExpertLink>
                        <Name lang="en">Epstein-Barr Virus-related tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="20753">
                            <OrphaCode>289644</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289644</ExpertLink>
                            <Name lang="en">Epstein-Barr virus-associated malignant lymphoproliferative disorder</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="12">
                            <ClassificationNode>
                              <Disorder id="3747">
                                <OrphaCode>543</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=543</ExpertLink>
                                <Name lang="en">Burkitt lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10593">
                                <OrphaCode>46135</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=46135</ExpertLink>
                                <Name lang="en">Primary central nervous system lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10631">
                                <OrphaCode>48686</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=48686</ExpertLink>
                                <Name lang="en">Primary effusion lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10952">
                                <OrphaCode>70568</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70568</ExpertLink>
                                <Name lang="en">Post-transplant lymphoproliferative disease</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11763">
                                <OrphaCode>86869</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86869</ExpertLink>
                                <Name lang="en">Lymphomatoid granulomatosis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11769">
                                <OrphaCode>86879</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86879</ExpertLink>
                                <Name lang="en">Extranodal nasal NK/T cell lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="13310">
                                <OrphaCode>98293</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98293</ExpertLink>
                                <Name lang="en">Hodgkin lymphoma</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="3739">
                                    <OrphaCode>391</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=391</ExpertLink>
                                    <Name lang="en">Classic Hodgkin lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="4">
                                    <ClassificationNode>
                                      <Disorder id="13860">
                                        <OrphaCode>98843</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98843</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, nodular sclerosis type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="13861">
                                        <OrphaCode>98844</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98844</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, mixed cellularity type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="13862">
                                        <OrphaCode>98845</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98845</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, lymphocyte-rich type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                    <ClassificationNode>
                                      <Disorder id="13863">
                                        <OrphaCode>98846</OrphaCode>
                                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98846</ExpertLink>
                                        <Name lang="en">Classic Hodgkin lymphoma, lymphocyte-depleted type</Name>
                                        <DisorderType id="21457">
                                          <Name lang="en">Histopathological subtype</Name>
                                        </DisorderType>
                                      </Disorder>
                                      <ClassificationNodeChildList count="0">
                                      </ClassificationNodeChildList>
                                    </ClassificationNode>
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11775">
                                    <OrphaCode>86893</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86893</ExpertLink>
                                    <Name lang="en">Nodular lymphocyte predominant Hodgkin lymphoma</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20756">
                                <OrphaCode>289661</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289661</ExpertLink>
                                <Name lang="en">Epstein-Barr virus-positive diffuse large B-cell lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20757">
                                <OrphaCode>289666</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289666</ExpertLink>
                                <Name lang="en">Plasmablastic lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21150">
                                <OrphaCode>300888</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=300888</ExpertLink>
                                <Name lang="en">Diffuse large B-cell lymphoma with chronic inflammation</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22361">
                                <OrphaCode>364033</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=364033</ExpertLink>
                                <Name lang="en">Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22362">
                                <OrphaCode>364039</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=364039</ExpertLink>
                                <Name lang="en">Hydroa vacciniforme-like lymphoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20754">
                            <OrphaCode>289651</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289651</ExpertLink>
                            <Name lang="en">Epstein-Barr Virus-associated carcinoma</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <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="20758">
                                <OrphaCode>289682</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289682</ExpertLink>
                                <Name lang="en">Lymphoepithelial-like carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21464">
                                <OrphaCode>313920</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=313920</ExpertLink>
                                <Name lang="en">Epstein-Barr virus-associated gastric carcinoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20755">
                            <OrphaCode>289656</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289656</ExpertLink>
                            <Name lang="en">Epstein-Barr Virus-associated mesenchymal tumor</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="10838">
                                <OrphaCode>64720</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=64720</ExpertLink>
                                <Name lang="en">Leiomyosarcoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11779">
                                <OrphaCode>86902</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86902</ExpertLink>
                                <Name lang="en">Follicular dendritic cell sarcoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20759">
                                <OrphaCode>289685</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289685</ExpertLink>
                                <Name lang="en">Myopericytoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23455">
                        <OrphaCode>443291</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=443291</ExpertLink>
                        <Name lang="en">HIV-associated cancer</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="20785">
                    <OrphaCode>290849</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=290849</ExpertLink>
                    <Name lang="en">Rare head and neck tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="4">
                    <ClassificationNode>
                      <Disorder id="13079">
                        <OrphaCode>98061</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98061</ExpertLink>
                        <Name lang="en">Rare otorhinolaryngologic tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="11">
                        <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="10898">
                            <OrphaCode>67037</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=67037</ExpertLink>
                            <Name lang="en">Squamous cell carcinoma of head and neck</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="5">
                            <ClassificationNode>
                              <Disorder id="25683">
                                <OrphaCode>494547</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494547</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the hypopharynx</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="25684">
                                <OrphaCode>494550</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494550</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the larynx</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="26030">
                                <OrphaCode>500464</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=500464</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the nasal cavity and paranasal sinuses</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="26034">
                                <OrphaCode>500478</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=500478</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of the oropharynx</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="26075">
                                <OrphaCode>502369</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=502369</ExpertLink>
                                <Name lang="en">Squamous cell carcinoma of oral cavity and lip</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="26073">
                                    <OrphaCode>502363</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=502363</ExpertLink>
                                    <Name lang="en">Squamous cell carcinoma of the oral cavity</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="26074">
                                    <OrphaCode>502366</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=502366</ExpertLink>
                                    <Name lang="en">Squamous cell carcinoma of the lip</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14655">
                            <OrphaCode>100083</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100083</ExpertLink>
                            <Name lang="en">Laryngeal neuroendocrine tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="14656">
                            <OrphaCode>100084</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100084</ExpertLink>
                            <Name lang="en">Middle ear neuroendocrine tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17031">
                            <OrphaCode>141077</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141077</ExpertLink>
                            <Name lang="en">Epignathus</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17037">
                            <OrphaCode>141107</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141107</ExpertLink>
                            <Name lang="en">Nasopharyngeal teratoma</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17038">
                            <OrphaCode>141112</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141112</ExpertLink>
                            <Name lang="en">Nasal glial heterotopia</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17039">
                            <OrphaCode>141115</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141115</ExpertLink>
                            <Name lang="en">Nasal ganglioglioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19728">
                            <OrphaCode>252175</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252175</ExpertLink>
                            <Name lang="en">Vestibular schwannoma</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20748">
                            <OrphaCode>289596</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289596</ExpertLink>
                            <Name lang="en">Juvenile nasopharyngeal angiofibroma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32073">
                            <OrphaCode>667678</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=667678</ExpertLink>
                            <Name lang="en">Intraoral basal cell carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20347">
                        <OrphaCode>276142</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276142</ExpertLink>
                        <Name lang="en">Rare tumor of salivary glands</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="20348">
                            <OrphaCode>276145</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276145</ExpertLink>
                            <Name lang="en">Malignant epithelial tumor of salivary glands</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="20349">
                            <OrphaCode>276148</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276148</ExpertLink>
                            <Name lang="en">Benign epithelial tumor of salivary glands</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21485">
                        <OrphaCode>314425</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314425</ExpertLink>
                        <Name lang="en">Rare odontogenic tumor</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="4">
                        <ClassificationNode>
                          <Disorder id="21483">
                            <OrphaCode>314419</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314419</ExpertLink>
                            <Name lang="en">Ameloblastoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="21484">
                            <OrphaCode>314422</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314422</ExpertLink>
                            <Name lang="en">Ameloblastic carcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23542">
                            <OrphaCode>447777</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=447777</ExpertLink>
                            <Name lang="en">Keratocystic odontogenic tumor</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32215">
                            <OrphaCode>689430</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=689430</ExpertLink>
                            <Name lang="en">Adenoid ameloblastoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32307">
                        <OrphaCode>696078</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=696078</ExpertLink>
                        <Name lang="en">Central giant cell granuloma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23447">
                    <OrphaCode>443167</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=443167</ExpertLink>
                    <Name lang="en">NUT midline carcinoma</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="31488">
                    <OrphaCode>626609</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=626609</ExpertLink>
                    <Name lang="en">Rare andrological tumor</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="2">
                    <ClassificationNode>
                      <Disorder id="22308">
                        <OrphaCode>363472</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363472</ExpertLink>
                        <Name lang="en">Tumor of testis and paratestis</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="18502">
                            <OrphaCode>206484</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=206484</ExpertLink>
                            <Name lang="en">Gonadoblastoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22309">
                            <OrphaCode>363478</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363478</ExpertLink>
                            <Name lang="en">Paratesticular adenocarcinoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22310">
                            <OrphaCode>363483</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363483</ExpertLink>
                            <Name lang="en">Testicular teratoma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22311">
                            <OrphaCode>363489</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363489</ExpertLink>
                            <Name lang="en">Sex cord-stromal tumor of testis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22313">
                            <OrphaCode>363504</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363504</ExpertLink>
                            <Name lang="en">Germ cell tumor of testis</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="3762">
                                <OrphaCode>842</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=842</ExpertLink>
                                <Name lang="en">Testicular seminomatous germ cell tumor</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14438">
                                <OrphaCode>99865</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99865</ExpertLink>
                                <Name lang="en">Spermatocytic seminoma</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22312">
                                <OrphaCode>363494</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363494</ExpertLink>
                                <Name lang="en">Non-seminomatous germ cell tumor of testis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32163">
                            <OrphaCode>685010</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=685010</ExpertLink>
                            <Name lang="en">Mesothelioma of the tunica vaginalis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22716">
                        <OrphaCode>398043</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398043</ExpertLink>
                        <Name lang="en">Malignant tumor of penis</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="22717">
                            <OrphaCode>398053</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398053</ExpertLink>
                            <Name lang="en">Adenocarcinoma of the penis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22718">
                            <OrphaCode>398058</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398058</ExpertLink>
                            <Name lang="en">Squamous cell carcinoma of the penis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="31593">
                    <OrphaCode>631251</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=631251</ExpertLink>
                    <Name lang="en">Cancer of unknown primary site</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
              </ClassificationNodeChildList>
            </ClassificationNode>
            <ClassificationNode>
              <Disorder id="16945">
                <OrphaCode>140162</OrphaCode>
                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=140162</ExpertLink>
                <Name lang="en">Inherited cancer-predisposing syndrome</Name>
                <DisorderType id="36561">
                  <Name lang="en">Category</Name>
                </DisorderType>
              </Disorder>
              <ClassificationNodeChildList count="44">
                <ClassificationNode>
                  <Disorder id="930">
                    <OrphaCode>638</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=638</ExpertLink>
                    <Name lang="en">Neurofibromatosis-Noonan syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="3560">
                    <OrphaCode>618</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=618</ExpertLink>
                    <Name lang="en">Familial melanoma</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="22495">
                    <OrphaCode>370396</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370396</ExpertLink>
                    <Name lang="en">Small cell carcinoma of the ovary</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="8593">
                    <OrphaCode>615</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=615</ExpertLink>
                    <Name lang="en">Familial atrial myxoma</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="207">
                    <OrphaCode>377</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=377</ExpertLink>
                    <Name lang="en">Gorlin syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="415">
                    <OrphaCode>1059</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1059</ExpertLink>
                    <Name lang="en">Blue rubber bleb nevus syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="477">
                    <OrphaCode>1775</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1775</ExpertLink>
                    <Name lang="en">Dyskeratosis congenita</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="2080">
                    <OrphaCode>2198</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2198</ExpertLink>
                    <Name lang="en">Palmoplantar keratoderma-esophageal carcinoma syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="2257">
                    <OrphaCode>296</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=296</ExpertLink>
                    <Name lang="en">Ollier disease</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="8531">
                    <OrphaCode>302</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=302</ExpertLink>
                    <Name lang="en">Inherited epidermodysplasia verruciformis</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="14322">
                    <OrphaCode>99749</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99749</ExpertLink>
                    <Name lang="en">Kostmann syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="17509">
                    <OrphaCode>163634</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=163634</ExpertLink>
                    <Name lang="en">Maffucci syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18230">
                    <OrphaCode>183422</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=183422</ExpertLink>
                    <Name lang="en">Polymalformative genetic syndrome with increased risk of developing cancer</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="47">
                    <ClassificationNode>
                      <Disorder id="253">
                        <OrphaCode>52</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=52</ExpertLink>
                        <Name lang="en">Alagille syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="19894">
                            <OrphaCode>261600</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=261600</ExpertLink>
                            <Name lang="en">Alagille syndrome due to 20p12 microdeletion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19895">
                            <OrphaCode>261619</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=261619</ExpertLink>
                            <Name lang="en">Alagille syndrome due to a JAG1 point mutation</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19896">
                            <OrphaCode>261629</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=261629</ExpertLink>
                            <Name lang="en">Alagille syndrome due to a NOTCH2 point mutation</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="254">
                        <OrphaCode>50</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=50</ExpertLink>
                        <Name lang="en">Aicardi syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="260">
                        <OrphaCode>116</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=116</ExpertLink>
                        <Name lang="en">Beckwith-Wiedemann syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="12700">
                            <OrphaCode>96076</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96076</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to 11p15 microduplication</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12817">
                            <OrphaCode>96193</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96193</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19155">
                            <OrphaCode>231117</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231117</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to imprinting defect of 11p15</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19156">
                            <OrphaCode>231120</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231120</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to CDKN1C mutation</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19158">
                            <OrphaCode>231127</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231127</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to 11p15 microdeletion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19159">
                            <OrphaCode>231130</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231130</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="279">
                        <OrphaCode>562</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=562</ExpertLink>
                        <Name lang="en">McCune-Albright syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="429">
                        <OrphaCode>124</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=124</ExpertLink>
                        <Name lang="en">Diamond-Blackfan anemia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="430">
                        <OrphaCode>125</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=125</ExpertLink>
                        <Name lang="en">Bloom syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="574">
                        <OrphaCode>3071</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3071</ExpertLink>
                        <Name lang="en">Costello syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="584">
                        <OrphaCode>813</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=813</ExpertLink>
                        <Name lang="en">Silver-Russell syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="12806">
                            <OrphaCode>96182</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96182</ExpertLink>
                            <Name lang="en">Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19160">
                            <OrphaCode>231137</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231137</ExpertLink>
                            <Name lang="en">Silver-Russell syndrome due to 7p11.2p13 microduplication</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19161">
                            <OrphaCode>231140</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231140</ExpertLink>
                            <Name lang="en">Silver-Russell syndrome due to an imprinting defect of 11p15</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19162">
                            <OrphaCode>231144</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231144</ExpertLink>
                            <Name lang="en">Silver-Russell syndrome due to 11p15 microduplication</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19163">
                            <OrphaCode>231147</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231147</ExpertLink>
                            <Name lang="en">Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22683">
                            <OrphaCode>397590</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=397590</ExpertLink>
                            <Name lang="en">Silver-Russell syndrome due to a point mutation</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="588">
                        <OrphaCode>821</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=821</ExpertLink>
                        <Name lang="en">Sotos syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="634">
                        <OrphaCode>84</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=84</ExpertLink>
                        <Name lang="en">Fanconi anemia</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="638">
                        <OrphaCode>191</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=191</ExpertLink>
                        <Name lang="en">Cockayne syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="4">
                        <ClassificationNode>
                          <Disorder id="1649">
                            <OrphaCode>1466</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1466</ExpertLink>
                            <Name lang="en">COFS syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12008">
                            <OrphaCode>90321</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90321</ExpertLink>
                            <Name lang="en">Cockayne syndrome type 1</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12009">
                            <OrphaCode>90322</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90322</ExpertLink>
                            <Name lang="en">Cockayne syndrome type 2</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12010">
                            <OrphaCode>90324</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90324</ExpertLink>
                            <Name lang="en">Cockayne syndrome type 3</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="660">
                        <OrphaCode>805</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=805</ExpertLink>
                        <Name lang="en">Tuberous sclerosis complex</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="912">
                        <OrphaCode>373</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=373</ExpertLink>
                        <Name lang="en">Simpson-Golabi-Behmel syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="960">
                        <OrphaCode>902</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=902</ExpertLink>
                        <Name lang="en">Werner syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1032">
                        <OrphaCode>500</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=500</ExpertLink>
                        <Name lang="en">Noonan syndrome with multiple lentigines</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1351">
                        <OrphaCode>1052</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1052</ExpertLink>
                        <Name lang="en">Mosaic variegated aneuploidy syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2033">
                        <OrphaCode>2128</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2128</ExpertLink>
                        <Name lang="en">Isolated hemihyperplasia</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2390">
                        <OrphaCode>2608</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2608</ExpertLink>
                        <Name lang="en">N syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2807">
                        <OrphaCode>798</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=798</ExpertLink>
                        <Name lang="en">Schinzel-Giedion syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2823">
                        <OrphaCode>647</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=647</ExpertLink>
                        <Name lang="en">Nijmegen breakage syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3253">
                        <OrphaCode>910</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=910</ExpertLink>
                        <Name lang="en">Xeroderma pigmentosum</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3474">
                        <OrphaCode>2849</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2849</ExpertLink>
                        <Name lang="en">Perlman syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3494">
                        <OrphaCode>882</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=882</ExpertLink>
                        <Name lang="en">Tyrosinemia type 1</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3552">
                        <OrphaCode>220</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=220</ExpertLink>
                        <Name lang="en">Denys-Drash syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3616">
                        <OrphaCode>347</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=347</ExpertLink>
                        <Name lang="en">Frasier syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="5536">
                        <OrphaCode>811</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=811</ExpertLink>
                        <Name lang="en">Shwachman-Diamond syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10664">
                        <OrphaCode>50944</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=50944</ExpertLink>
                        <Name lang="en">Schöpf-Schulz-Passarge syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10805">
                        <OrphaCode>60040</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=60040</ExpertLink>
                        <Name lang="en">Megalencephaly-capillary malformation-polymicrogyria syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12020">
                        <OrphaCode>90342</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90342</ExpertLink>
                        <Name lang="en">Xeroderma pigmentosum variant</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14385">
                        <OrphaCode>99812</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99812</ExpertLink>
                        <Name lang="en">LIG4 syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17621">
                        <OrphaCode>166113</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=166113</ExpertLink>
                        <Name lang="en">Bazex syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17815">
                        <OrphaCode>169079</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=169079</ExpertLink>
                        <Name lang="en">Cernunnos-XLF deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18903">
                        <OrphaCode>220295</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=220295</ExpertLink>
                        <Name lang="en">Xeroderma pigmentosum-Cockayne syndrome complex</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18930">
                        <OrphaCode>221016</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=221016</ExpertLink>
                        <Name lang="en">Rothmund-Thomson syndrome type 2</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19345">
                        <OrphaCode>240760</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=240760</ExpertLink>
                        <Name lang="en">Nijmegen breakage syndrome-like disorder</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19631">
                        <OrphaCode>251347</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251347</ExpertLink>
                        <Name lang="en">Ataxia-telangiectasia-like disorder</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20473">
                        <OrphaCode>280558</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280558</ExpertLink>
                        <Name lang="en">Warsaw breakage syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21218">
                        <OrphaCode>306498</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306498</ExpertLink>
                        <Name lang="en">PTEN hamartoma tumor syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="243">
                            <OrphaCode>201</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=201</ExpertLink>
                            <Name lang="en">Cowden syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="1473">
                            <OrphaCode>109</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=109</ExpertLink>
                            <Name lang="en">Bannayan-Riley-Ruvalcaba syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2675">
                            <OrphaCode>2969</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2969</ExpertLink>
                            <Name lang="en">Proteus-like syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10867">
                            <OrphaCode>65285</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=65285</ExpertLink>
                            <Name lang="en">Lhermitte-Duclos disease</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="16690">
                            <OrphaCode>137608</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137608</ExpertLink>
                            <Name lang="en">Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22353">
                        <OrphaCode>363972</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363972</ExpertLink>
                        <Name lang="en">Noonan syndrome-like disorder with juvenile myelomonocytic leukemia</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23365">
                        <OrphaCode>438134</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=438134</ExpertLink>
                        <Name lang="en">PCNA-related progressive neurodegenerative photosensitivity syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="104">
                        <OrphaCode>100</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=100</ExpertLink>
                        <Name lang="en">Ataxia-telangiectasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="144">
                        <OrphaCode>906</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=906</ExpertLink>
                        <Name lang="en">Wiskott-Aldrich syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="151">
                        <OrphaCode>783</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=783</ExpertLink>
                        <Name lang="en">Rubinstein-Taybi syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="22127">
                            <OrphaCode>353277</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=353277</ExpertLink>
                            <Name lang="en">Rubinstein-Taybi syndrome due to CREBBP mutations</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22128">
                            <OrphaCode>353281</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=353281</ExpertLink>
                            <Name lang="en">Rubinstein-Taybi syndrome due to 16p13.3 microdeletion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22129">
                            <OrphaCode>353284</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=353284</ExpertLink>
                            <Name lang="en">Rubinstein-Taybi syndrome due to EP300 haploinsufficiency</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="206">
                        <OrphaCode>648</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=648</ExpertLink>
                        <Name lang="en">Noonan syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="230">
                        <OrphaCode>893</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=893</ExpertLink>
                        <Name lang="en">WAGR syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="233">
                        <OrphaCode>2869</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2869</ExpertLink>
                        <Name lang="en">Peutz-Jeghers syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="235">
                        <OrphaCode>794</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=794</ExpertLink>
                        <Name lang="en">Saethre-Chotzen syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="19153">
                    <OrphaCode>231108</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231108</ExpertLink>
                    <Name lang="en">Rhabdoid tumor predisposition syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="19731">
                    <OrphaCode>252202</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252202</ExpertLink>
                    <Name lang="en">Constitutional mismatch repair deficiency syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="19732">
                    <OrphaCode>252206</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=252206</ExpertLink>
                    <Name lang="en">Melanoma and neural system tumor syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="20371">
                    <OrphaCode>276399</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=276399</ExpertLink>
                    <Name lang="en">Familial multinodular goiter</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</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="20737">
                    <OrphaCode>289539</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289539</ExpertLink>
                    <Name lang="en">BAP1-related tumor predisposition syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="20874">
                    <OrphaCode>293822</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=293822</ExpertLink>
                    <Name lang="en">MITF-related melanoma and renal cell carcinoma predisposition syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="21457">
                    <OrphaCode>313846</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=313846</ExpertLink>
                    <Name lang="en">Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="21648">
                    <OrphaCode>319328</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319328</ExpertLink>
                    <Name lang="en">Inherited renal cancer-predisposing syndrome</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="13">
                    <ClassificationNode>
                      <Disorder id="99">
                        <OrphaCode>892</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=892</ExpertLink>
                        <Name lang="en">Von Hippel-Lindau disease</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="230">
                        <OrphaCode>893</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=893</ExpertLink>
                        <Name lang="en">WAGR syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="260">
                        <OrphaCode>116</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=116</ExpertLink>
                        <Name lang="en">Beckwith-Wiedemann syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="12700">
                            <OrphaCode>96076</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96076</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to 11p15 microduplication</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12817">
                            <OrphaCode>96193</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96193</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19155">
                            <OrphaCode>231117</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231117</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to imprinting defect of 11p15</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19156">
                            <OrphaCode>231120</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231120</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to CDKN1C mutation</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19158">
                            <OrphaCode>231127</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231127</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to 11p15 microdeletion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19159">
                            <OrphaCode>231130</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=231130</ExpertLink>
                            <Name lang="en">Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="660">
                        <OrphaCode>805</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=805</ExpertLink>
                        <Name lang="en">Tuberous sclerosis complex</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3474">
                        <OrphaCode>2849</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2849</ExpertLink>
                        <Name lang="en">Perlman syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <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="8649">
                        <OrphaCode>523</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=523</ExpertLink>
                        <Name lang="en">Hereditary leiomyomatosis and renal cell cancer</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="10607">
                        <OrphaCode>47044</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=47044</ExpertLink>
                        <Name lang="en">Hereditary papillary renal cell carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12883">
                        <OrphaCode>97290</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97290</ExpertLink>
                        <Name lang="en">Familial papillary thyroid carcinoma with renal papillary neoplasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14453">
                        <OrphaCode>99880</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99880</ExpertLink>
                        <Name lang="en">Hyperparathyroidism-jaw tumor syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21658">
                        <OrphaCode>319462</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319462</ExpertLink>
                        <Name lang="en">Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22928">
                        <OrphaCode>404476</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404476</ExpertLink>
                        <Name lang="en">Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23138">
                        <OrphaCode>422526</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=422526</ExpertLink>
                        <Name lang="en">Hereditary clear cell renal cell carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="22197">
                    <OrphaCode>357027</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=357027</ExpertLink>
                    <Name lang="en">Hereditary retinoblastoma</Name>
                    <DisorderType id="21450">
                      <Name lang="en">Clinical subtype</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="22939">
                    <OrphaCode>404560</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404560</ExpertLink>
                    <Name lang="en">Familial atypical multiple mole melanoma syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23208">
                    <OrphaCode>425003</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=425003</ExpertLink>
                    <Name lang="en">Inherited digestive cancer-predisposing syndrome</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="6">
                    <ClassificationNode>
                      <Disorder id="121">
                        <OrphaCode>652</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652</ExpertLink>
                        <Name lang="en">Multiple endocrine neoplasia type 1</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="906">
                        <OrphaCode>653</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=653</ExpertLink>
                        <Name lang="en">Multiple endocrine neoplasia type 2</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="19538">
                            <OrphaCode>247698</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247698</ExpertLink>
                            <Name lang="en">Multiple endocrine neoplasia type 2A</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19539">
                            <OrphaCode>247709</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247709</ExpertLink>
                            <Name lang="en">Multiple endocrine neoplasia type 2B</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="14205">
                        <OrphaCode>99361</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99361</ExpertLink>
                        <Name lang="en">Isolated familial medullary thyroid carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="15001">
                        <OrphaCode>104010</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=104010</ExpertLink>
                        <Name lang="en">Intestinal polyposis syndrome</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="15">
                        <ClassificationNode>
                          <Disorder id="105">
                            <OrphaCode>733</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=733</ExpertLink>
                            <Name lang="en">Familial adenomatous polyposis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="233">
                            <OrphaCode>2869</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2869</ExpertLink>
                            <Name lang="en">Peutz-Jeghers syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="243">
                            <OrphaCode>201</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=201</ExpertLink>
                            <Name lang="en">Cowden syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="848">
                            <OrphaCode>2929</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2929</ExpertLink>
                            <Name lang="en">Juvenile polyposis syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="11125">
                                <OrphaCode>79076</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79076</ExpertLink>
                                <Name lang="en">Juvenile polyposis of infancy</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="21951">
                                <OrphaCode>329971</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=329971</ExpertLink>
                                <Name lang="en">Generalized juvenile polyposis/juvenile polyposis coli</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="1473">
                            <OrphaCode>109</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=109</ExpertLink>
                            <Name lang="en">Bannayan-Riley-Ruvalcaba syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="2646">
                            <OrphaCode>2930</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2930</ExpertLink>
                            <Name lang="en">Cronkhite-Canada syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17145">
                            <OrphaCode>157794</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=157794</ExpertLink>
                            <Name lang="en">Hereditary mixed polyposis syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17146">
                            <OrphaCode>157798</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=157798</ExpertLink>
                            <Name lang="en">Serrated polyposis syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18912">
                            <OrphaCode>220460</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=220460</ExpertLink>
                            <Name lang="en">Attenuated familial adenomatous polyposis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19549">
                            <OrphaCode>247798</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=247798</ExpertLink>
                            <Name lang="en">MUTYH-related polyposis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19893">
                            <OrphaCode>261584</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=261584</ExpertLink>
                            <Name lang="en">5q22 microdeletion syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22850">
                            <OrphaCode>401911</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=401911</ExpertLink>
                            <Name lang="en">AXIN2-related polyposis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23548">
                            <OrphaCode>447877</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=447877</ExpertLink>
                            <Name lang="en">Polymerase proofreading-related polyposis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23666">
                            <OrphaCode>454840</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=454840</ExpertLink>
                            <Name lang="en">NTHL1-related polyposis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="25215">
                            <OrphaCode>480536</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=480536</ExpertLink>
                            <Name lang="en">MSH3-related polyposis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23469">
                        <OrphaCode>443909</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=443909</ExpertLink>
                        <Name lang="en">Hereditary nonpolyposis colon cancer</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="3245">
                            <OrphaCode>144</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=144</ExpertLink>
                            <Name lang="en">Lynch syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23409">
                            <OrphaCode>440437</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=440437</ExpertLink>
                            <Name lang="en">Familial colorectal cancer Type X</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23679">
                        <OrphaCode>456333</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=456333</ExpertLink>
                        <Name lang="en">Hereditary neuroendocrine tumor of small intestine</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23233">
                    <OrphaCode>431149</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=431149</ExpertLink>
                    <Name lang="en">Combined immunodeficiency due to OX40 deficiency</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23322">
                    <OrphaCode>435953</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=435953</ExpertLink>
                    <Name lang="en">Progeroid features-hepatocellular carcinoma predisposition syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23554">
                    <OrphaCode>447961</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=447961</ExpertLink>
                    <Name lang="en">Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="28611">
                    <OrphaCode>568056</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=568056</ExpertLink>
                    <Name lang="en">Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="29440">
                    <OrphaCode>589746</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=589746</ExpertLink>
                    <Name lang="en">Inherited gynecological cancer-predisposing syndrome</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="4">
                    <ClassificationNode>
                      <Disorder id="233">
                        <OrphaCode>2869</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2869</ExpertLink>
                        <Name lang="en">Peutz-Jeghers syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="243">
                        <OrphaCode>201</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=201</ExpertLink>
                        <Name lang="en">Cowden syndrome</Name>
                        <DisorderType id="21450">
                          <Name lang="en">Clinical subtype</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="8649">
                        <OrphaCode>523</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=523</ExpertLink>
                        <Name lang="en">Hereditary leiomyomatosis and renal cell cancer</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23469">
                        <OrphaCode>443909</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=443909</ExpertLink>
                        <Name lang="en">Hereditary nonpolyposis colon cancer</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="3245">
                            <OrphaCode>144</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=144</ExpertLink>
                            <Name lang="en">Lynch syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23409">
                            <OrphaCode>440437</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=440437</ExpertLink>
                            <Name lang="en">Familial colorectal cancer Type X</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="31413">
                    <OrphaCode>619340</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=619340</ExpertLink>
                    <Name lang="en">Inherited hematologic cancer-predisposing syndrome</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="8">
                    <ClassificationNode>
                      <Disorder id="196">
                        <OrphaCode>524</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=524</ExpertLink>
                        <Name lang="en">Li-Fraumeni syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="206">
                        <OrphaCode>648</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=648</ExpertLink>
                        <Name lang="en">Noonan syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1032">
                        <OrphaCode>500</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=500</ExpertLink>
                        <Name lang="en">Noonan syndrome with multiple lentigines</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="11012">
                        <OrphaCode>71290</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=71290</ExpertLink>
                        <Name lang="en">Familial platelet disorder with associated myeloid malignancy</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21659">
                        <OrphaCode>319465</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319465</ExpertLink>
                        <Name lang="en">Inherited acute myeloid leukemia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="25413">
                        <OrphaCode>488647</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=488647</ExpertLink>
                        <Name lang="en">DDX41-related hematologic malignancy predisposition syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32358">
                        <OrphaCode>697385</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=697385</ExpertLink>
                        <Name lang="en">Combined immunodeficiency-cancer predisposing syndrome due to AIOLOS deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="32404">
                            <OrphaCode>699596</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=699596</ExpertLink>
                            <Name lang="en">Combined immunodeficiency-hypogammaglobulinemia-cancer predisposing syndrome due to AIOLOS deficiency</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32403">
                            <OrphaCode>699593</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=699593</ExpertLink>
                            <Name lang="en">Combined immunodeficiency-lymphopenia-cancer predisposing syndrome due to AIOLOS deficiency</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32365">
                        <OrphaCode>697414</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=697414</ExpertLink>
                        <Name lang="en">Early-onset combined immunodeficiency with low Ig due to dominant negative IKAROS mutation</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="31695">
                    <OrphaCode>634518</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=634518</ExpertLink>
                    <Name lang="en">Neurofibromatosis/schwannomatosis</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="6">
                    <ClassificationNode>
                      <Disorder id="183">
                        <OrphaCode>637</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=637</ExpertLink>
                        <Name lang="en">Full NF2-related schwannomatosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="185">
                        <OrphaCode>636</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=636</ExpertLink>
                        <Name lang="en">Neurofibromatosis type 1</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="12945">
                            <OrphaCode>97685</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97685</ExpertLink>
                            <Name lang="en">17q11 microdeletion syndrome</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22341">
                            <OrphaCode>363700</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363700</ExpertLink>
                            <Name lang="en">Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion</Name>
                            <DisorderType id="21443">
                              <Name lang="en">Etiological subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12482">
                        <OrphaCode>93921</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93921</ExpertLink>
                        <Name lang="en">Full schwannomatosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31691">
                        <OrphaCode>634461</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=634461</ExpertLink>
                        <Name lang="en">Mosaic neurofibromatosis type 1</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31692">
                        <OrphaCode>634475</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=634475</ExpertLink>
                        <Name lang="en">Mosaic NF2-related schwannomatosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31693">
                        <OrphaCode>634492</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=634492</ExpertLink>
                        <Name lang="en">Mosaic schwannomatosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="31991">
                    <OrphaCode>661526</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=661526</ExpertLink>
                    <Name lang="en">MBD4-related tumor predisposition syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="32037">
                    <OrphaCode>664450</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=664450</ExpertLink>
                    <Name lang="en">Inherited cancer-predisposing lymphoproliferative syndrome</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="25">
                    <ClassificationNode>
                      <Disorder id="282">
                        <OrphaCode>540</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=540</ExpertLink>
                        <Name lang="en">Familial hemophagocytic lymphohistiocytosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3035">
                        <OrphaCode>3453</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3453</ExpertLink>
                        <Name lang="en">Autoimmune polyendocrinopathy type 1</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3468">
                        <OrphaCode>3261</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3261</ExpertLink>
                        <Name lang="en">Autoimmune lymphoproliferative syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19269">
                        <OrphaCode>238505</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=238505</ExpertLink>
                        <Name lang="en">Combined immunodeficiency due to CD27 deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20165">
                        <OrphaCode>268114</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=268114</ExpertLink>
                        <Name lang="en">RAS-associated autoimmune leukoproliferative disease</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20316">
                        <OrphaCode>275523</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=275523</ExpertLink>
                        <Name lang="en">Dianzani autoimmune lymphoproliferative disease</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21230">
                        <OrphaCode>306550</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=306550</ExpertLink>
                        <Name lang="en">FADD-related immunodeficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="21585">
                        <OrphaCode>317476</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=317476</ExpertLink>
                        <Name lang="en">XMEN</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="22628">
                        <OrphaCode>391487</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=391487</ExpertLink>
                        <Name lang="en">STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23115">
                        <OrphaCode>420573</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=420573</ExpertLink>
                        <Name lang="en">EBV-induced lymphoproliferative disease due to CTPS1 deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23329">
                        <OrphaCode>436159</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=436159</ExpertLink>
                        <Name lang="en">Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23366">
                        <OrphaCode>438159</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=438159</ExpertLink>
                        <Name lang="en">STAT3-related early-onset multisystem autoimmune disease</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="27963">
                        <OrphaCode>538931</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=538931</ExpertLink>
                        <Name lang="en">X-linked lymphoproliferative disease due to SAP deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="27968">
                        <OrphaCode>538958</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=538958</ExpertLink>
                        <Name lang="en">EBV-induced lymphoproliferative disease due to CD70 deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="27969">
                        <OrphaCode>538963</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=538963</ExpertLink>
                        <Name lang="en">Combined immunodeficiency due to ITK deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="28036">
                        <OrphaCode>542301</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=542301</ExpertLink>
                        <Name lang="en">EBV-induced lymphoproliferative disease due to CARMIL2 deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="31418">
                        <OrphaCode>619948</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=619948</ExpertLink>
                        <Name lang="en">Early-onset autoimmunity-autoinflammation-immunodeficiency syndrome due to SOCS1 haploinsufficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32049">
                        <OrphaCode>664699</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=664699</ExpertLink>
                        <Name lang="en">EBV-induced lymphoproliferative disease due to RASGRP1 deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32051">
                        <OrphaCode>664711</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=664711</ExpertLink>
                        <Name lang="en">EBV-induced lymphoproliferative disease due to PRKCD deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32053">
                        <OrphaCode>664726</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=664726</ExpertLink>
                        <Name lang="en">EBV-induced lymphoproliferative disease due to CD137 deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32054">
                        <OrphaCode>664729</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=664729</ExpertLink>
                        <Name lang="en">EBV-induced lymphoproliferative disease due to TET2 deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32298">
                        <OrphaCode>695172</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=695172</ExpertLink>
                        <Name lang="en">Combined immunodeficiency due to dimerization defective IKAROS mutation</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32305">
                        <OrphaCode>695807</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=695807</ExpertLink>
                        <Name lang="en">Immunodeficiency-systemic inflammation-lymphoma predisposition syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32327">
                        <OrphaCode>696874</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=696874</ExpertLink>
                        <Name lang="en">NFKB1-related immune dysregulation</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32359">
                        <OrphaCode>697389</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=697389</ExpertLink>
                        <Name lang="en">Combined immunodeficiency due to HELIOS deficiency</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </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="3384">
                    <OrphaCode>145</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=145</ExpertLink>
                    <Name lang="en">Hereditary breast and/or ovarian cancer syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="2389">
                    <OrphaCode>1359</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1359</ExpertLink>
                    <Name lang="en">Carney complex</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="16888">
                    <OrphaCode>139411</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=139411</ExpertLink>
                    <Name lang="en">Carney triad</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
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                <ClassificationNode>
                  <Disorder id="21661">
                    <OrphaCode>319487</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319487</ExpertLink>
                    <Name lang="en">Familial papillary or follicular thyroid carcinoma</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
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                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
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                <ClassificationNode>
                  <Disorder id="21662">
                    <OrphaCode>319494</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319494</ExpertLink>
                    <Name lang="en">Familial nonmedullary thyroid carcinoma</Name>
                    <DisorderType id="21436">
                      <Name lang="en">Clinical group</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="2">
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                      <Disorder id="12883">
                        <OrphaCode>97290</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97290</ExpertLink>
                        <Name lang="en">Familial papillary thyroid carcinoma with renal papillary neoplasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
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                    <ClassificationNode>
                      <Disorder id="21661">
                        <OrphaCode>319487</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=319487</ExpertLink>
                        <Name lang="en">Familial papillary or follicular thyroid carcinoma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
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                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="12880">
                    <OrphaCode>97286</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97286</ExpertLink>
                    <Name lang="en">Carney-Stratakis syndrome</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
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                  </Disorder>
                  <ClassificationNodeChildList count="0">
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                <ClassificationNode>
                  <Disorder id="21470">
                    <OrphaCode>314022</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314022</ExpertLink>
                    <Name lang="en">Gastric adenocarcinoma and proximal polyposis of the stomach</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
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                <ClassificationNode>
                  <Disorder id="8758">
                    <OrphaCode>26106</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=26106</ExpertLink>
                    <Name lang="en">Hereditary diffuse gastric cancer</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="8775">
                    <OrphaCode>29072</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=29072</ExpertLink>
                    <Name lang="en">Hereditary pheochromocytoma-paraganglioma</Name>
                    <DisorderType id="21394">
                      <Name lang="en">Disease</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
                </ClassificationNode>
              </ClassificationNodeChildList>
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