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                                <Name lang="en">X-linked severe syndromic thoracic aortic aneurysm and dissection</Name>
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                                <Name lang="en">Arterial tortuosity syndrome</Name>
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                                <OrphaCode>286</OrphaCode>
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                                <Name lang="en">Vascular Ehlers-Danlos syndrome</Name>
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                                <Name lang="en">Loeys-Dietz syndrome</Name>
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                                <Name lang="en">Familial thoracic aortic aneurysm and aortic dissection</Name>
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                                <Name lang="en">Familial aortic dissection</Name>
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                            <OrphaCode>289601</OrphaCode>
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                            <Name lang="en">Hereditary arterial and articular multiple calcification syndrome</Name>
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                            <OrphaCode>314718</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=314718</ExpertLink>
                            <Name lang="en">Lethal arteriopathy syndrome due to fibulin-4 deficiency</Name>
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                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90349</ExpertLink>
                            <Name lang="en">Autosomal recessive cutis laxa type 1</Name>
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                        <OrphaCode>280062</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=280062</ExpertLink>
                        <Name lang="en">Calciphylaxis</Name>
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                            <Name lang="en">Calciphylaxis cutis</Name>
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                            <Name lang="en">Visceral calciphylaxis</Name>
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                              <Name lang="en">Clinical subtype</Name>
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                        <Name lang="en">Susac syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="10704">
                    <OrphaCode>52759</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=52759</ExpertLink>
                    <Name lang="en">Vasculitis</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="5">
                    <ClassificationNode>
                      <Disorder id="17095">
                        <OrphaCode>156140</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=156140</ExpertLink>
                        <Name lang="en">Predominantly large-vessel vasculitis</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="8759">
                            <OrphaCode>26137</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=26137</ExpertLink>
                            <Name lang="en">Juvenile temporal arteritis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="703">
                            <OrphaCode>117</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=117</ExpertLink>
                            <Name lang="en">Behçet disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="806">
                            <OrphaCode>3287</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3287</ExpertLink>
                            <Name lang="en">Takayasu arteritis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="876">
                            <OrphaCode>397</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=397</ExpertLink>
                            <Name lang="en">Giant cell arteritis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3333">
                            <OrphaCode>1467</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1467</ExpertLink>
                            <Name lang="en">Cogan syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19069">
                            <OrphaCode>228116</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=228116</ExpertLink>
                            <Name lang="en">Hughes-Stovin syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17096">
                        <OrphaCode>156143</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=156143</ExpertLink>
                        <Name lang="en">Predominantly medium-vessel vasculitis</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="788">
                            <OrphaCode>2331</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2331</ExpertLink>
                            <Name lang="en">Kawasaki disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3403">
                            <OrphaCode>767</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=767</ExpertLink>
                            <Name lang="en">Polyarteritis nodosa</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="23387">
                                <OrphaCode>439737</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=439737</ExpertLink>
                                <Name lang="en">Primary polyarteritis nodosa</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="23386">
                                    <OrphaCode>439729</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=439729</ExpertLink>
                                    <Name lang="en">Cutaneous polyarteritis nodosa</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23389">
                                    <OrphaCode>439755</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=439755</ExpertLink>
                                    <Name lang="en">Single-organ polyarteritis nodosa</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="23390">
                                    <OrphaCode>439762</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=439762</ExpertLink>
                                    <Name lang="en">Systemic polyarteritis nodosa</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23388">
                                <OrphaCode>439746</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=439746</ExpertLink>
                                <Name lang="en">Secondary polyarteritis nodosa</Name>
                                <DisorderType id="21450">
                                  <Name lang="en">Clinical subtype</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="10414">
                            <OrphaCode>36258</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=36258</ExpertLink>
                            <Name lang="en">Buerger disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17015">
                            <OrphaCode>140989</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=140989</ExpertLink>
                            <Name lang="en">Primary angiitis of the central nervous system</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="22938">
                            <OrphaCode>404553</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=404553</ExpertLink>
                            <Name lang="en">Deficiency of adenosine deaminase 2</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="29783">
                            <OrphaCode>596753</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=596753</ExpertLink>
                            <Name lang="en">VEXAS syndrome</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="17097">
                        <OrphaCode>156146</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=156146</ExpertLink>
                        <Name lang="en">Predominantly small-vessel vasculitis</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="17015">
                            <OrphaCode>140989</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=140989</ExpertLink>
                            <Name lang="en">Primary angiitis of the central nervous system</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="747">
                            <OrphaCode>375</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=375</ExpertLink>
                            <Name lang="en">Anti-glomerular basement membrane disease</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17098">
                            <OrphaCode>156149</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=156149</ExpertLink>
                            <Name lang="en">Immune complex mediated vasculitis</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="5">
                            <ClassificationNode>
                              <Disorder id="749">
                                <OrphaCode>761</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=761</ExpertLink>
                                <Name lang="en">Immunoglobulin A vasculitis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8613">
                                <OrphaCode>889</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=889</ExpertLink>
                                <Name lang="en">Cutaneous small vessel vasculitis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10428">
                                <OrphaCode>36412</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=36412</ExpertLink>
                                <Name lang="en">Hypocomplementemic urticarial vasculitis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11918">
                                <OrphaCode>90000</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90000</ExpertLink>
                                <Name lang="en">Erythema elevatum diutinum</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="12115">
                                <OrphaCode>91138</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=91138</ExpertLink>
                                <Name lang="en">Cryoglobulinemic vasculitis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="12396">
                                    <OrphaCode>93554</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93554</ExpertLink>
                                    <Name lang="en">Mixed cryoglobulinemia type II</Name>
                                    <DisorderType id="21443">
                                      <Name lang="en">Etiological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12397">
                                    <OrphaCode>93555</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=93555</ExpertLink>
                                    <Name lang="en">Mixed cryoglobulinemia type III</Name>
                                    <DisorderType id="21443">
                                      <Name lang="en">Etiological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17099">
                            <OrphaCode>156152</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=156152</ExpertLink>
                            <Name lang="en">Anti-neutrophil cytoplasmic antibody-associated vasculitis</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="745">
                                <OrphaCode>183</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=183</ExpertLink>
                                <Name lang="en">Eosinophilic granulomatosis with polyangiitis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="753">
                                <OrphaCode>727</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=727</ExpertLink>
                                <Name lang="en">Microscopic polyangiitis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="759">
                                <OrphaCode>900</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=900</ExpertLink>
                                <Name lang="en">Granulomatosis with polyangiitis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23209">
                            <OrphaCode>425120</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=425120</ExpertLink>
                            <Name lang="en">STING-associated vasculopathy with onset in infancy</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="19629">
                        <OrphaCode>251328</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251328</ExpertLink>
                        <Name lang="en">Unclassified vasculitis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23521">
                        <OrphaCode>445197</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=445197</ExpertLink>
                        <Name lang="en">Secondary vasculitis</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="10626">
                            <OrphaCode>48435</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=48435</ExpertLink>
                            <Name lang="en">Postinfectious vasculitis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="19628">
                            <OrphaCode>251325</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251325</ExpertLink>
                            <Name lang="en">Drug-induced vasculitis</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="10560">
                <OrphaCode>68419</OrphaCode>
                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=68419</ExpertLink>
                <Name lang="en">Rare vascular anomaly</Name>
                <DisorderType id="36561">
                  <Name lang="en">Category</Name>
                </DisorderType>
              </Disorder>
              <ClassificationNodeChildList count="10">
                <ClassificationNode>
                  <Disorder id="18716">
                    <OrphaCode>211266</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211266</ExpertLink>
                    <Name lang="en">Fast-flow vascular malformation</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="4">
                    <ClassificationNode>
                      <Disorder id="32633">
                        <OrphaCode>715762</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715762</ExpertLink>
                        <Name lang="en">Unifocal fast-flow vascular malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="32494">
                            <OrphaCode>707944</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=707944</ExpertLink>
                            <Name lang="en">Peripheral fast-flow vascular malformation</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="32503">
                                <OrphaCode>708051</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=708051</ExpertLink>
                                <Name lang="en">Peripheral congenital arteriovenous fistula</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32497">
                                <OrphaCode>708007</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=708007</ExpertLink>
                                <Name lang="en">Intramuscular fast-flow vascular anomaly</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32502">
                                <OrphaCode>708046</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=708046</ExpertLink>
                                <Name lang="en">Peripheral arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32630">
                            <OrphaCode>715744</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715744</ExpertLink>
                            <Name lang="en">Fast-flow vascular malformation of the central nervous system</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="32631">
                                <OrphaCode>715750</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715750</ExpertLink>
                                <Name lang="en">Intracranial fast-flow vascular malformation</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="6">
                                <ClassificationNode>
                                  <Disorder id="10604">
                                    <OrphaCode>46724</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=46724</ExpertLink>
                                    <Name lang="en">Brain arteriovenous malformation</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32600">
                                    <OrphaCode>715292</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715292</ExpertLink>
                                    <Name lang="en">Brain pial arteriovenous fistula</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32603">
                                    <OrphaCode>715318</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715318</ExpertLink>
                                    <Name lang="en">Acquired intracranial dural arteriovenous fistula</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="12895">
                                    <OrphaCode>97339</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97339</ExpertLink>
                                    <Name lang="en">Dural sinus malformation with arteriovenous shunt</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32234">
                                    <OrphaCode>692271</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=692271</ExpertLink>
                                    <Name lang="en">Cerebral proliferative angiopathy</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="1352">
                                    <OrphaCode>1053</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1053</ExpertLink>
                                    <Name lang="en">Vein of Galen malformation</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32588">
                                <OrphaCode>715025</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715025</ExpertLink>
                                <Name lang="en">Spinal fast-flow vascular malformation</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="32599">
                                    <OrphaCode>715284</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715284</ExpertLink>
                                    <Name lang="en">Spinal cord arteriovenous malformation</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32601">
                                    <OrphaCode>715302</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715302</ExpertLink>
                                    <Name lang="en">Spinal pial arteriovenous fistula</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32602">
                                    <OrphaCode>715307</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715307</ExpertLink>
                                    <Name lang="en">Acquired spinal dural arteriovenous fistula</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32604">
                                    <OrphaCode>715326</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715326</ExpertLink>
                                    <Name lang="en">Spinal epidural arteriovenous malformation</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32605">
                                    <OrphaCode>715331</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715331</ExpertLink>
                                    <Name lang="en">Paraspinal arteriovenous malformation</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32632">
                            <OrphaCode>715757</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715757</ExpertLink>
                            <Name lang="en">Metameric fast-flow vascular malformation</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="10743">
                                <OrphaCode>53721</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=53721</ExpertLink>
                                <Name lang="en">Spinal arteriovenous metameric syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="17057">
                                <OrphaCode>141189</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141189</ExpertLink>
                                <Name lang="en">Cerebrofacial arteriovenous metameric syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32254">
                            <OrphaCode>693855</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693855</ExpertLink>
                            <Name lang="en">Visceral arteriovenous malformation</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="9">
                            <ClassificationNode>
                              <Disorder id="32253">
                                <OrphaCode>693846</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693846</ExpertLink>
                                <Name lang="en">Hepatic arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32252">
                                <OrphaCode>693839</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693839</ExpertLink>
                                <Name lang="en">Renal arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32251">
                                <OrphaCode>693832</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693832</ExpertLink>
                                <Name lang="en">Gastrointestinal tract arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32255">
                                <OrphaCode>693863</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693863</ExpertLink>
                                <Name lang="en">Splenic arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32249">
                                <OrphaCode>693815</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693815</ExpertLink>
                                <Name lang="en">Uterine arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32250">
                                <OrphaCode>693826</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693826</ExpertLink>
                                <Name lang="en">Pancreatic arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32256">
                                <OrphaCode>693869</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693869</ExpertLink>
                                <Name lang="en">Gallblader arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32257">
                                <OrphaCode>693872</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693872</ExpertLink>
                                <Name lang="en">Urinary tract arteriovenous malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3441">
                                <OrphaCode>2038</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2038</ExpertLink>
                                <Name lang="en">Pulmonary arteriovenous malformation</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32577">
                            <OrphaCode>714698</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714698</ExpertLink>
                            <Name lang="en">Arteriovenous malformation of the thoraco-abdominal-pelvic cavity</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="4">
                            <ClassificationNode>
                              <Disorder id="32579">
                                <OrphaCode>714709</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714709</ExpertLink>
                                <Name lang="en">Mediastinal arteriovenous malformation</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32581">
                                <OrphaCode>714726</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714726</ExpertLink>
                                <Name lang="en">Retroperitoneal arteriovenous malformation</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32580">
                                <OrphaCode>714715</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714715</ExpertLink>
                                <Name lang="en">Pelvic arteriovenous malformation</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="32578">
                                <OrphaCode>714702</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714702</ExpertLink>
                                <Name lang="en">Abdominal arteriovenous malformation</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="16702">
                        <OrphaCode>137667</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137667</ExpertLink>
                        <Name lang="en">Capillary malformation-arteriovenous malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="32265">
                            <OrphaCode>693907</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693907</ExpertLink>
                            <Name lang="en">RASA1-related capillary malformation-arteriovenous malformation</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32266">
                            <OrphaCode>693912</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693912</ExpertLink>
                            <Name lang="en">EPHB4-related capillary malformation-arteriovenous malformation</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="236">
                        <OrphaCode>774</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=774</ExpertLink>
                        <Name lang="en">Hereditary hemorrhagic telangiectasia</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12004">
                        <OrphaCode>90307</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90307</ExpertLink>
                        <Name lang="en">Parkes Weber syndrome</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18714">
                    <OrphaCode>211252</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211252</ExpertLink>
                    <Name lang="en">Slow-flow malformation, venous type</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="8">
                    <ClassificationNode>
                      <Disorder id="32607">
                        <OrphaCode>715339</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715339</ExpertLink>
                        <Name lang="en">Multifocal peripheral venous malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="5">
                        <ClassificationNode>
                          <Disorder id="2266">
                            <OrphaCode>2451</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2451</ExpertLink>
                            <Name lang="en">Mucocutaneous venous malformations</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32586">
                            <OrphaCode>714806</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714806</ExpertLink>
                            <Name lang="en">Multifocal sporadic venous malformation</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11573">
                            <OrphaCode>83454</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=83454</ExpertLink>
                            <Name lang="en">Glomuvenous malformation</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="16965">
                            <OrphaCode>140436</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=140436</ExpertLink>
                            <Name lang="en">Familial intraosseous vascular malformation</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</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</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32606">
                        <OrphaCode>715334</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715334</ExpertLink>
                        <Name lang="en">Unifocal peripheral venous malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="7">
                        <ClassificationNode>
                          <Disorder id="32585">
                            <OrphaCode>714785</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714785</ExpertLink>
                            <Name lang="en">Unifocal sporadic venous malformation</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32638">
                            <OrphaCode>715923</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715923</ExpertLink>
                            <Name lang="en">Intraosseous venous malformation</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="24017">
                            <OrphaCode>464318</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=464318</ExpertLink>
                            <Name lang="en">Verrucous hemangioma</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32415">
                            <OrphaCode>699683</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=699683</ExpertLink>
                            <Name lang="en">Fibro-adipose vascular anomaly</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32189">
                            <OrphaCode>688523</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=688523</ExpertLink>
                            <Name lang="en">Splenic venous malformation</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="18807">
                            <OrphaCode>217008</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=217008</ExpertLink>
                            <Name lang="en">Segmental venous malformation</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11573">
                            <OrphaCode>83454</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=83454</ExpertLink>
                            <Name lang="en">Glomuvenous malformation</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32719">
                        <OrphaCode>717564</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717564</ExpertLink>
                        <Name lang="en">Dural sinus malformation without arteriovenous shunt</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</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="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="32582">
                        <OrphaCode>714734</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714734</ExpertLink>
                        <Name lang="en">Sinus pericranii</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="18935">
                        <OrphaCode>221061</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=221061</ExpertLink>
                        <Name lang="en">Familial cerebral cavernous malformation</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12005">
                        <OrphaCode>90308</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90308</ExpertLink>
                        <Name lang="en">Capillary-lymphatic-venous malformation with segmental distribution</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18713">
                    <OrphaCode>211247</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211247</ExpertLink>
                    <Name lang="en">Rare capillary malformation</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="10">
                    <ClassificationNode>
                      <Disorder id="12588">
                        <OrphaCode>95429</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95429</ExpertLink>
                        <Name lang="en">Angioma serpiginosum</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="2606">
                        <OrphaCode>2875</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2875</ExpertLink>
                        <Name lang="en">Phakomatosis pigmentovascularis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="11509">
                            <OrphaCode>79483</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79483</ExpertLink>
                            <Name lang="en">Phakomatosis cesioflammea</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11510">
                            <OrphaCode>79484</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79484</ExpertLink>
                            <Name lang="en">Phakomatosis cesiomarmorata</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="11511">
                            <OrphaCode>79485</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79485</ExpertLink>
                            <Name lang="en">Phakomatosis spilorosea</Name>
                            <DisorderType id="21450">
                              <Name lang="en">Clinical subtype</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="20901">
                        <OrphaCode>294016</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=294016</ExpertLink>
                        <Name lang="en">Microcephaly-capillary malformation syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="1222">
                        <OrphaCode>624</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=624</ExpertLink>
                        <Name lang="en">Familial multiple nevi flammei</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="23759">
                        <OrphaCode>458830</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458830</ExpertLink>
                        <Name lang="en">Rare capillary malformation with associated anomalies</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="2464">
                            <OrphaCode>2703</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2703</ExpertLink>
                            <Name lang="en">Port-wine nevi-mega cisterna magna-hydrocephalus syndrome</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</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>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32611">
                        <OrphaCode>715446</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715446</ExpertLink>
                        <Name lang="en">Geographic pattern capillary malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="32608">
                            <OrphaCode>715345</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715345</ExpertLink>
                            <Name lang="en">Isolated geographic pattern capillary malformation</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32613">
                            <OrphaCode>715460</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715460</ExpertLink>
                            <Name lang="en">Syndromic geographic pattern capillary malformation</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <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="17810">
                                <OrphaCode>168984</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=168984</ExpertLink>
                                <Name lang="en">CLAPO syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="12005">
                                <OrphaCode>90308</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90308</ExpertLink>
                                <Name lang="en">Capillary-lymphatic-venous malformation with segmental distribution</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32612">
                        <OrphaCode>715453</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715453</ExpertLink>
                        <Name lang="en">Reticulated capillary malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="32609">
                            <OrphaCode>715353</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715353</ExpertLink>
                            <Name lang="en">Isolated reticulated capillary malformation</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</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="32583">
                            <OrphaCode>714737</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=714737</ExpertLink>
                            <Name lang="en">Diffuse capillary malformation with overgrowth</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32614">
                        <OrphaCode>715463</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715463</ExpertLink>
                        <Name lang="en">Low resistance capillary malformation</Name>
                        <DisorderType id="21436">
                          <Name lang="en">Clinical group</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="32610">
                            <OrphaCode>715359</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715359</ExpertLink>
                            <Name lang="en">Isolated low resistance capillary malformation</Name>
                            <DisorderType id="21415">
                              <Name lang="en">Morphological anomaly</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="32615">
                            <OrphaCode>715466</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=715466</ExpertLink>
                            <Name lang="en">Syndromic low resistance capillary malformation</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="12004">
                                <OrphaCode>90307</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90307</ExpertLink>
                                <Name lang="en">Parkes Weber syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="16702">
                                <OrphaCode>137667</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=137667</ExpertLink>
                                <Name lang="en">Capillary malformation-arteriovenous malformation</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="32265">
                                    <OrphaCode>693907</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693907</ExpertLink>
                                    <Name lang="en">RASA1-related capillary malformation-arteriovenous malformation</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="32266">
                                    <OrphaCode>693912</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=693912</ExpertLink>
                                    <Name lang="en">EPHB4-related capillary malformation-arteriovenous malformation</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="591">
                        <OrphaCode>3205</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3205</ExpertLink>
                        <Name lang="en">Sturge-Weber syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="454">
                        <OrphaCode>1556</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1556</ExpertLink>
                        <Name lang="en">Cutis marmorata telangiectatica congenita</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="18715">
                    <OrphaCode>211255</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211255</ExpertLink>
                    <Name lang="en">Slow-flow malformation, lymphatic type</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="2">
                    <ClassificationNode>
                      <Disorder id="11097">
                        <OrphaCode>77240</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=77240</ExpertLink>
                        <Name lang="en">Primary lymphedema</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="3">
                        <ClassificationNode>
                          <Disorder id="28607">
                            <OrphaCode>568041</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=568041</ExpertLink>
                            <Name lang="en">Primary lymphedema without systemic or visceral involvement</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="2">
                            <ClassificationNode>
                              <Disorder id="780">
                                <OrphaCode>2416</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2416</ExpertLink>
                                <Name lang="en">Congenital primary lymphedema without systemic or visceral involvement</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="5">
                                <ClassificationNode>
                                  <Disorder id="20949">
                                    <OrphaCode>295000</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=295000</ExpertLink>
                                    <Name lang="en">Amniotic band syndrome</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11478">
                                    <OrphaCode>79452</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79452</ExpertLink>
                                    <Name lang="en">Milroy disease</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="28655">
                                    <OrphaCode>569821</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=569821</ExpertLink>
                                    <Name lang="en">Congenital primary lymphedema of Gordon</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="2336">
                                    <OrphaCode>2526</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2526</ExpertLink>
                                    <Name lang="en">Microcephaly-lymphedema-chorioretinopathy syndrome</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="1992">
                                    <OrphaCode>2077</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2077</ExpertLink>
                                    <Name lang="en">German syndrome</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="20760">
                                <OrphaCode>289825</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=289825</ExpertLink>
                                <Name lang="en">Late-onset primary lymphedema without systemic or visceral involvement</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="6">
                                <ClassificationNode>
                                  <Disorder id="437">
                                    <OrphaCode>1414</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1414</ExpertLink>
                                    <Name lang="en">Cholestasis-lymphedema syndrome</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="10305">
                                    <OrphaCode>33001</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=33001</ExpertLink>
                                    <Name lang="en">Lymphedema-distichiasis syndrome</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="28610">
                                    <OrphaCode>568051</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=568051</ExpertLink>
                                    <Name lang="en">GJC2-related late-onset primary lymphedema</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14158">
                                    <OrphaCode>99141</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99141</ExpertLink>
                                    <Name lang="en">Lymphedema-posterior choanal atresia syndrome</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="11993">
                                    <OrphaCode>90186</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=90186</ExpertLink>
                                    <Name lang="en">Meige disease</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="28654">
                                    <OrphaCode>569816</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=569816</ExpertLink>
                                    <Name lang="en">CELSR1-related late-onset primary lymphedema</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="28608">
                            <OrphaCode>568044</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=568044</ExpertLink>
                            <Name lang="en">Primary lymphedema with systemic or visceral involvement</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="9">
                            <ClassificationNode>
                              <Disorder id="1716">
                                <OrphaCode>1563</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1563</ExpertLink>
                                <Name lang="en">Dahlberg-Borer-Newcomer syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="1397">
                                <OrphaCode>1116</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1116</ExpertLink>
                                <Name lang="en">Aplasia cutis congenita-intestinal lymphangiectasia syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="2036">
                                <OrphaCode>2136</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2136</ExpertLink>
                                <Name lang="en">Hennekam syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28613">
                                <OrphaCode>568065</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=568065</ExpertLink>
                                <Name lang="en">EPHB4-related lymphatic-related hydrops fetalis</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28612">
                                <OrphaCode>568062</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=568062</ExpertLink>
                                <Name lang="en">PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis</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="6520">
                                <OrphaCode>662</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662</ExpertLink>
                                <Name lang="en">Lymphedema with yellow nails</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10936">
                                <OrphaCode>69735</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=69735</ExpertLink>
                                <Name lang="en">Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11788">
                                <OrphaCode>86915</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86915</ExpertLink>
                                <Name lang="en">Lymphedema-atrial septal defects-facial changes syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="28609">
                            <OrphaCode>568047</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=568047</ExpertLink>
                            <Name lang="en">Disorder with multisystemic involvement and primary lymphedema</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="13">
                            <ClassificationNode>
                              <Disorder id="25364">
                                <OrphaCode>487796</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=487796</ExpertLink>
                                <Name lang="en">Takenouchi-Kosaki syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="94">
                                <OrphaCode>324</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=324</ExpertLink>
                                <Name lang="en">Fabry disease</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="44">
                                <OrphaCode>881</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=881</ExpertLink>
                                <Name lang="en">Turner syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="14199">
                                    <OrphaCode>99226</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99226</ExpertLink>
                                    <Name lang="en">Monosomy X syndrome</Name>
                                    <DisorderType id="21443">
                                      <Name lang="en">Etiological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14200">
                                    <OrphaCode>99228</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99228</ExpertLink>
                                    <Name lang="en">Mosaic monosomy X syndrome</Name>
                                    <DisorderType id="21443">
                                      <Name lang="en">Etiological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14210">
                                    <OrphaCode>99413</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99413</ExpertLink>
                                    <Name lang="en">Turner syndrome due to structural X chromosome anomalies</Name>
                                    <DisorderType id="21443">
                                      <Name lang="en">Etiological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="1559">
                                <OrphaCode>1340</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1340</ExpertLink>
                                <Name lang="en">Cardiofaciocutaneous syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3214">
                                <OrphaCode>1655</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1655</ExpertLink>
                                <Name lang="en">Müllerian derivatives-lymphangiectasia-polydactyly syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="2573">
                                <OrphaCode>2836</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2836</ExpertLink>
                                <Name lang="en">PEHO syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10630">
                                <OrphaCode>48652</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=48652</ExpertLink>
                                <Name lang="en">Phelan-McDermid syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="31993">
                                    <OrphaCode>662172</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662172</ExpertLink>
                                    <Name lang="en">Phelan-McDermid syndrome due to SHANK3 mutation</Name>
                                    <DisorderType id="21443">
                                      <Name lang="en">Etiological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="31992">
                                    <OrphaCode>662169</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662169</ExpertLink>
                                    <Name lang="en">Phelan-McDermid syndrome due to 22q13.3 deletion</Name>
                                    <DisorderType id="21443">
                                      <Name lang="en">Etiological subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="10922">
                                <OrphaCode>69088</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=69088</ExpertLink>
                                <Name lang="en">Hypohidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="2471">
                                <OrphaCode>2710</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2710</ExpertLink>
                                <Name lang="en">Oculodentodigital dysplasia</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14380">
                                <OrphaCode>99807</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99807</ExpertLink>
                                <Name lang="en">PEHO-like syndrome</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</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="1727">
                                <OrphaCode>742</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=742</ExpertLink>
                                <Name lang="en">Prolidase deficiency</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="3547">
                        <OrphaCode>2415</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2415</ExpertLink>
                        <Name lang="en">Isolated rare lymphatic malformation</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="14158">
                            <OrphaCode>99141</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99141</ExpertLink>
                            <Name lang="en">Lymphedema-posterior choanal atresia syndrome</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="23760">
                            <OrphaCode>458833</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458833</ExpertLink>
                            <Name lang="en">Common cystic lymphatic malformation</Name>
                            <DisorderType id="21436">
                              <Name lang="en">Clinical group</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="11515">
                                <OrphaCode>79489</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79489</ExpertLink>
                                <Name lang="en">Macrocystic lymphatic malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="11516">
                                <OrphaCode>79490</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=79490</ExpertLink>
                                <Name lang="en">Microcystic lymphatic malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="23755">
                                <OrphaCode>458792</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458792</ExpertLink>
                                <Name lang="en">Mixed cystic lymphatic malformation</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="17061">
                            <OrphaCode>141209</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141209</ExpertLink>
                            <Name lang="en">Diffuse lymphatic malformation</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="8684">
                            <OrphaCode>73</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=73</ExpertLink>
                            <Name lang="en">Gorham-Stout disease</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="24019">
                            <OrphaCode>464329</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=464329</ExpertLink>
                            <Name lang="en">Kaposiform lymphangiomatosis</Name>
                            <DisorderType id="21394">
                              <Name lang="en">Disease</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <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>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="32720">
                    <OrphaCode>717582</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717582</ExpertLink>
                    <Name lang="en">Coagulation abnormality associated with a vascular anomaly</Name>
                    <DisorderType id="21436">
                      <Name lang="en">Clinical group</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="4">
                    <ClassificationNode>
                      <Disorder id="3399">
                        <OrphaCode>2330</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2330</ExpertLink>
                        <Name lang="en">Kasabach-Merritt phenomenon</Name>
                        <DisorderType id="21429">
                          <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32721">
                        <OrphaCode>717585</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717585</ExpertLink>
                        <Name lang="en">Kasabach-Merritt-like phenomenon</Name>
                        <DisorderType id="21429">
                          <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32722">
                        <OrphaCode>717588</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717588</ExpertLink>
                        <Name lang="en">Localized intravascular coagulation</Name>
                        <DisorderType id="21429">
                          <Name lang="en">Particular clinical situation in a disease or syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32723">
                        <OrphaCode>717593</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717593</ExpertLink>
                        <Name lang="en">Disseminated intravascular coagulation associated with a vascular anomaly</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="18717">
                    <OrphaCode>211277</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211277</ExpertLink>
                    <Name lang="en">Complex vascular malformation with associated anomalies</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="4">
                    <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="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="11787">
                        <OrphaCode>86914</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=86914</ExpertLink>
                        <Name lang="en">Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</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>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23761">
                    <OrphaCode>458837</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458837</ExpertLink>
                    <Name lang="en">Rare combined vascular malformation</Name>
                    <DisorderType id="21436">
                      <Name lang="en">Clinical group</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="5">
                    <ClassificationNode>
                      <Disorder id="32726">
                        <OrphaCode>717611</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717611</ExpertLink>
                        <Name lang="en">Capillary-venous malformation</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32725">
                        <OrphaCode>717605</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717605</ExpertLink>
                        <Name lang="en">Capillary-lymphatic malformation</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32724">
                        <OrphaCode>717598</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717598</ExpertLink>
                        <Name lang="en">Lymphatic-venous malformation</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32727">
                        <OrphaCode>717619</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=717619</ExpertLink>
                        <Name lang="en">Capillary-lymphatic-venous malformation</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="24017">
                        <OrphaCode>464318</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=464318</ExpertLink>
                        <Name lang="en">Verrucous hemangioma</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
                <ClassificationNode>
                  <Disorder id="23763">
                    <OrphaCode>458844</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=458844</ExpertLink>
                    <Name lang="en">Rare vascular malformation of major vessels</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="6">
                    <ClassificationNode>
                      <Disorder id="1299">
                        <OrphaCode>981</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=981</ExpertLink>
                        <Name lang="en">Internal carotid absence</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="13741">
                        <OrphaCode>98724</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98724</ExpertLink>
                        <Name lang="en">Congenital anomaly of the great arteries</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="6">
                        <ClassificationNode>
                          <Disorder id="3428">
                            <OrphaCode>1132</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1132</ExpertLink>
                            <Name lang="en">Aortic arch defects</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="7">
                            <ClassificationNode>
                              <Disorder id="14092">
                                <OrphaCode>99075</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99075</ExpertLink>
                                <Name lang="en">Encircling double aortic arch</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14093">
                                <OrphaCode>99076</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99076</ExpertLink>
                                <Name lang="en">Persistent fifth aortic arch</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14094">
                                <OrphaCode>99077</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99077</ExpertLink>
                                <Name lang="en">Kommerell diverticulum</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14095">
                                <OrphaCode>99078</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99078</ExpertLink>
                                <Name lang="en">Neuhauser anomaly</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14096">
                                <OrphaCode>99079</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99079</ExpertLink>
                                <Name lang="en">Cervical aortic arch</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14098">
                                <OrphaCode>99081</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99081</ExpertLink>
                                <Name lang="en">Right aortic arch</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14099">
                                <OrphaCode>99082</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99082</ExpertLink>
                                <Name lang="en">Dysphagia lusoria</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="3462">
                            <OrphaCode>185</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=185</ExpertLink>
                            <Name lang="en">Scimitar syndrome</Name>
                            <DisorderType id="21401">
                              <Name lang="en">Malformation syndrome</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="0">
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="12609">
                            <OrphaCode>95485</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95485</ExpertLink>
                            <Name lang="en">Arterial duct anomaly</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="12610">
                                <OrphaCode>95486</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95486</ExpertLink>
                                <Name lang="en">Premature closure of the arterial duct</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14089">
                                <OrphaCode>99072</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99072</ExpertLink>
                                <Name lang="en">Congenital patent ductus arteriosus aneurysm</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="24163">
                                <OrphaCode>466729</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=466729</ExpertLink>
                                <Name lang="en">Familial patent arterial duct</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13735">
                            <OrphaCode>98718</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98718</ExpertLink>
                            <Name lang="en">Aortic malformation</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="8">
                            <ClassificationNode>
                              <Disorder id="2859">
                                <OrphaCode>3193</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3193</ExpertLink>
                                <Name lang="en">Supravalvular aortic stenosis</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3434">
                                <OrphaCode>1456</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1456</ExpertLink>
                                <Name lang="en">Middle aortic syndrome</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="28051">
                                <OrphaCode>542568</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=542568</ExpertLink>
                                <Name lang="en">Quadricuspid aortic valve</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3435">
                                <OrphaCode>1457</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1457</ExpertLink>
                                <Name lang="en">Coarctation of aorta</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3448">
                                <OrphaCode>2299</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2299</ExpertLink>
                                <Name lang="en">Aortic arch interruption</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3454">
                                <OrphaCode>3092</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3092</ExpertLink>
                                <Name lang="en">Fixed subaortic stenosis</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="14068">
                                    <OrphaCode>99051</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99051</ExpertLink>
                                    <Name lang="en">Discrete fixed membranous subaortic stenosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14069">
                                    <OrphaCode>99052</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99052</ExpertLink>
                                    <Name lang="en">Discrete fibromuscular subaortic stenosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14070">
                                    <OrphaCode>99053</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99053</ExpertLink>
                                    <Name lang="en">Tunnel subaortic stenosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3455">
                                <OrphaCode>3093</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3093</ExpertLink>
                                <Name lang="en">Congenital aortic valve stenosis</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="12595">
                                    <OrphaCode>95448</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95448</ExpertLink>
                                    <Name lang="en">Congenital aortic valve atresia</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14754">
                                    <OrphaCode>101043</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101043</ExpertLink>
                                    <Name lang="en">Congenital aortic valve dysplasia</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="22877">
                                <OrphaCode>402075</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=402075</ExpertLink>
                                <Name lang="en">Familial bicuspid aortic valve</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13736">
                            <OrphaCode>98719</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98719</ExpertLink>
                            <Name lang="en">Pulmonary artery or pulmonary branch anomaly</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="7">
                            <ClassificationNode>
                              <Disorder id="1455">
                                <OrphaCode>1208</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1208</ExpertLink>
                                <Name lang="en">Pulmonary atresia-intact ventricular septum syndrome</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3424">
                                <OrphaCode>982</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=982</ExpertLink>
                                <Name lang="en">Pulmonary valve agenesis</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14065">
                                    <OrphaCode>99048</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99048</ExpertLink>
                                    <Name lang="en">Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14834">
                                    <OrphaCode>101206</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101206</ExpertLink>
                                    <Name lang="en">Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3425">
                                <OrphaCode>980</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=980</ExpertLink>
                                <Name lang="en">Absence of the pulmonary artery</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3460">
                                <OrphaCode>3189</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3189</ExpertLink>
                                <Name lang="en">Congenital pulmonary valvar stenosis</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="3">
                                <ClassificationNode>
                                  <Disorder id="3461">
                                    <OrphaCode>3190</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3190</ExpertLink>
                                    <Name lang="en">Subpulmonary stenosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="8606">
                                    <OrphaCode>3192</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3192</ExpertLink>
                                    <Name lang="en">Supravalvular pulmonary stenosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14071">
                                    <OrphaCode>99054</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99054</ExpertLink>
                                    <Name lang="en">Valvular pulmonary stenosis</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="8600">
                                <OrphaCode>1676</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1676</ExpertLink>
                                <Name lang="en">Idiopathic pulmonary artery dilatation</Name>
                                <DisorderType id="21394">
                                  <Name lang="en">Disease</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14100">
                                <OrphaCode>99083</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99083</ExpertLink>
                                <Name lang="en">Pulmonary artery hypoplasia</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="14101">
                                <OrphaCode>99084</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99084</ExpertLink>
                                <Name lang="en">Peripheral pulmonary stenosis</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13742">
                            <OrphaCode>98725</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98725</ExpertLink>
                            <Name lang="en">Ascending aorta anomaly</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="3426">
                                <OrphaCode>1054</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1054</ExpertLink>
                                <Name lang="en">Aneurysm of sinus of Valsalva</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3455">
                                <OrphaCode>3093</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3093</ExpertLink>
                                <Name lang="en">Congenital aortic valve stenosis</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="12595">
                                    <OrphaCode>95448</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95448</ExpertLink>
                                    <Name lang="en">Congenital aortic valve atresia</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14754">
                                    <OrphaCode>101043</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=101043</ExpertLink>
                                    <Name lang="en">Congenital aortic valve dysplasia</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3465">
                                <OrphaCode>3400</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3400</ExpertLink>
                                <Name lang="en">Aorto-ventricular tunnel</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14087">
                                    <OrphaCode>99070</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99070</ExpertLink>
                                    <Name lang="en">Aorto-right ventricular tunnel</Name>
                                    <DisorderType id="21450">
                                      <Name lang="en">Clinical subtype</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14088">
                                    <OrphaCode>99071</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99071</ExpertLink>
                                    <Name lang="en">Aorto-left ventricular tunnel</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="22277">
                        <OrphaCode>363189</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=363189</ExpertLink>
                        <Name lang="en">Congenital anomaly of the great veins</Name>
                        <DisorderType id="36561">
                          <Name lang="en">Category</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="2">
                        <ClassificationNode>
                          <Disorder id="3453">
                            <OrphaCode>3091</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3091</ExpertLink>
                            <Name lang="en">Congenital systemic veins anomaly</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="5">
                            <ClassificationNode>
                              <Disorder id="12622">
                                <OrphaCode>95498</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95498</ExpertLink>
                                <Name lang="en">Congenital anomaly of superior vena cava</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="7">
                                <ClassificationNode>
                                  <Disorder id="14127">
                                    <OrphaCode>99110</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99110</ExpertLink>
                                    <Name lang="en">Right superior vena cava connecting to left-sided atrium</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="31901">
                                    <OrphaCode>652668</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652668</ExpertLink>
                                    <Name lang="en">Primary superior vena cava aneurysm</Name>
                                    <DisorderType id="21401">
                                      <Name lang="en">Malformation syndrome</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14131">
                                    <OrphaCode>99114</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99114</ExpertLink>
                                    <Name lang="en">Agenesis of the superior vena cava</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14128">
                                    <OrphaCode>99111</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99111</ExpertLink>
                                    <Name lang="en">Persistent left superior vena cava connecting to the roof of left-sided atrium</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14130">
                                    <OrphaCode>99113</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99113</ExpertLink>
                                    <Name lang="en">Subaortic course of innominate vein</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14126">
                                    <OrphaCode>99109</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99109</ExpertLink>
                                    <Name lang="en">Persistent left superior vena cava connecting through coronary sinus to left-sided atrium</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14129">
                                    <OrphaCode>99112</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99112</ExpertLink>
                                    <Name lang="en">Absence of innominate vein</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="12623">
                                <OrphaCode>95499</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95499</ExpertLink>
                                <Name lang="en">Congenital anomaly of the inferior vena cava</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="6">
                                <ClassificationNode>
                                  <Disorder id="14136">
                                    <OrphaCode>99119</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99119</ExpertLink>
                                    <Name lang="en">Right inferior vena cava connecting to left-sided atrium</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14137">
                                    <OrphaCode>99120</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99120</ExpertLink>
                                    <Name lang="en">Persistent eustachian valve</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14139">
                                    <OrphaCode>99122</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99122</ExpertLink>
                                    <Name lang="en">Congenital stenosis of the inferior vena cava</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14140">
                                    <OrphaCode>99123</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99123</ExpertLink>
                                    <Name lang="en">Inferior vena cava interruption without azygos continuation</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="31902">
                                    <OrphaCode>652678</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=652678</ExpertLink>
                                    <Name lang="en">Primary inferior vena cava aneurysm</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14138">
                                    <OrphaCode>99121</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99121</ExpertLink>
                                    <Name lang="en">Azygos continuation of the inferior vena cava</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="12624">
                                <OrphaCode>95500</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95500</ExpertLink>
                                <Name lang="en">Congenital anomaly of the coronary sinus</Name>
                                <DisorderType id="36561">
                                  <Name lang="en">Category</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14134">
                                    <OrphaCode>99117</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99117</ExpertLink>
                                    <Name lang="en">Coronary sinus stenosis</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14135">
                                    <OrphaCode>99118</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99118</ExpertLink>
                                    <Name lang="en">Coronary sinus atresia</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="12631">
                                <OrphaCode>95507</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=95507</ExpertLink>
                                <Name lang="en">Congenital anomaly of hepatic vein</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="25214">
                                <OrphaCode>480531</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=480531</ExpertLink>
                                <Name lang="en">Congenital portosystemic shunt</Name>
                                <DisorderType id="21415">
                                  <Name lang="en">Morphological anomaly</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                        <ClassificationNode>
                          <Disorder id="13746">
                            <OrphaCode>98729</OrphaCode>
                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=98729</ExpertLink>
                            <Name lang="en">Congenital pulmonary veins anomaly</Name>
                            <DisorderType id="36561">
                              <Name lang="en">Category</Name>
                            </DisorderType>
                          </Disorder>
                          <ClassificationNodeChildList count="3">
                            <ClassificationNode>
                              <Disorder id="2772">
                                <OrphaCode>3090</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3090</ExpertLink>
                                <Name lang="en">Congenital pulmonary venous return anomaly</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14141">
                                    <OrphaCode>99124</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99124</ExpertLink>
                                    <Name lang="en">Congenital partial pulmonary venous return anomaly</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="14142">
                                    <OrphaCode>99125</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99125</ExpertLink>
                                    <Name lang="en">Congenital total pulmonary venous return anomaly</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3462">
                                <OrphaCode>185</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=185</ExpertLink>
                                <Name lang="en">Scimitar syndrome</Name>
                                <DisorderType id="21401">
                                  <Name lang="en">Malformation syndrome</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="0">
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                            <ClassificationNode>
                              <Disorder id="3459">
                                <OrphaCode>3188</OrphaCode>
                                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3188</ExpertLink>
                                <Name lang="en">Congenital pulmonary veins atresia or stenosis</Name>
                                <DisorderType id="21436">
                                  <Name lang="en">Clinical group</Name>
                                </DisorderType>
                              </Disorder>
                              <ClassificationNodeChildList count="2">
                                <ClassificationNode>
                                  <Disorder id="14143">
                                    <OrphaCode>99126</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99126</ExpertLink>
                                    <Name lang="en">Congenital pulmonary vein atresia</Name>
                                    <DisorderType id="21415">
                                      <Name lang="en">Morphological anomaly</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                                <ClassificationNode>
                                  <Disorder id="31729">
                                    <OrphaCode>642071</OrphaCode>
                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=642071</ExpertLink>
                                    <Name lang="en">Primary pulmonary vein stenosis</Name>
                                    <DisorderType id="21394">
                                      <Name lang="en">Disease</Name>
                                    </DisorderType>
                                  </Disorder>
                                  <ClassificationNodeChildList count="0">
                                  </ClassificationNodeChildList>
                                </ClassificationNode>
                              </ClassificationNodeChildList>
                            </ClassificationNode>
                          </ClassificationNodeChildList>
                        </ClassificationNode>
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="12937">
                        <OrphaCode>97598</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=97598</ExpertLink>
                        <Name lang="en">Congenital renal artery stenosis</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="32386">
                        <OrphaCode>698260</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=698260</ExpertLink>
                        <Name lang="en">Carotid web</Name>
                        <DisorderType id="21394">
                          <Name lang="en">Disease</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                    <ClassificationNode>
                      <Disorder id="25672">
                        <OrphaCode>494424</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=494424</ExpertLink>
                        <Name lang="en">Extracranial carotid artery aneurysm</Name>
                        <DisorderType id="21415">
                          <Name lang="en">Morphological anomaly</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </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="17">
                        <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>
                        <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 capillary malformation</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="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="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>
                            <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>
                          </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 haemangioma</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 haemangioma</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 haemangioma</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="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="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="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="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="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="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="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="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="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>
                            <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>
                          </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="6">
                        <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="18712">
                    <OrphaCode>211243</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=211243</ExpertLink>
                    <Name lang="en">Simple vascular malformation</Name>
                    <DisorderType id="36561">
                      <Name lang="en">Category</Name>
                    </DisorderType>
                  </Disorder>
                  <ClassificationNodeChildList count="1">
                    <ClassificationNode>
                      <Disorder id="32269">
                        <OrphaCode>694228</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=694228</ExpertLink>
                        <Name lang="en">Congenital intrahepatic arterioportal fistula</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
                        </DisorderType>
                      </Disorder>
                      <ClassificationNodeChildList count="0">
                      </ClassificationNodeChildList>
                    </ClassificationNode>
                  </ClassificationNodeChildList>
                </ClassificationNode>
              </ClassificationNodeChildList>
            </ClassificationNode>
          </ClassificationNodeChildList>
        </ClassificationNode>
      </ClassificationNodeRootList>
    </Classification>
  </ClassificationList>
</JDBOR>
