{"orpha":211277,"name":"Syndromic combined vascular malformation","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Complex vascular malformation with associated anomalie"],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-211277/","orphanet_url":"https://www.orpha.net/en/disease/detail/211277","names":{"fr":{"name":"Malformation vasculaire combinée syndromique","synonyms":["Malformation vasculaire complexe avec anomalies associées"]},"de":{"name":"Syndromale kombinierte vaskuläre Fehlbildung","synonyms":["Komplexe vaskuläre Malformation mit begleitender Anomalie","Hämangiolymphangiom","Syndromale kombinierte vaskuläre Malformation"]},"es":{"name":"Malformación vascular combinada sindrómica","synonyms":["Malformación vascular completa con anomalías asociadas"]},"it":{"name":"Malformazione vascolare combinata sindromica","synonyms":["Malformazione vascolare complessa con anomalie associate"]},"nl":{"name":"Syndromale gecombineerde vasculaire malformatie","synonyms":["Syndromale gecombineerde vaatmalformatie","Complexe vasculaire malformatie met geassocieerde anomalie"]},"pt":{"name":"Malformação vascular complexa/combinada"},"pl":{"name":"Złożona - mieszna malformacja naczyniowa","synonyms":["Complex vascular malformation with associated anomalie"]},"cs":{"name":"Komplexní vaskulární malformace s přidruženými anomáliemi","synonyms":["Hemangiolymfangiom"]},"uk":{"name":"Складна судинна вада розвитку з супутніми аномаліями","synonyms":["Гемангіолімфангіома"]},"zh":{"name":"复杂血管畸形伴相关异常","synonyms":["血管淋巴管瘤"]},"tr":{"name":"İlişkili anomaliler ile seyreden kompleks vasküler malformasyon","synonyms":["Hemanjiyolenfanjiyom"]}},"xrefs":[{"source":"MONDO","code":"16235","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679799","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":458837,"name":"Rare combined vascular malformation","classifications":[147,198]}],"children":[{"orpha":86914,"name":"Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome","type":"Malformation syndrome"},{"orpha":728584,"name":"PIK3CA-related overgrowth spectrum disorder with vascular malformation","type":"Clinical group"},{"orpha":744,"name":"Proteus syndrome","type":"Malformation syndrome"},{"orpha":137608,"name":"Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome","type":"Clinical subtype"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}