{"orpha":458830,"name":"Rare capillary malformation with associated anomalies","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-458830/","orphanet_url":"https://www.orpha.net/en/disease/detail/458830","names":{"fr":{"name":"Malformation capillaire rare avec anomalies associées"},"de":{"name":"Seltene kapilläre Fehlbildung mit assoziierten Anomalien"},"es":{"name":"Malformación capilar rara con anomalías asociadas"},"it":{"name":"Malformazione capillare con anomalie associate"},"nl":{"name":"Zeldzame capillaire malformatie met geassocieerde anomalieën"},"pt":{"name":"Malformação capilar com anomalias associadas"},"pl":{"name":"Rzadka malformacja naczyniowa z wadami towarzyszącymi"},"cs":{"name":"Vzácná kapilární malformace s asociovanými anomáliemi"},"uk":{"name":"Рідкісна капілярна мальформація з супутніми аномаліями"},"zh":{"name":"罕见毛细血管畸形及相关异常"},"tr":{"name":"İlişkili anomaliler ile seyreden nadir kılcal damar malformasyonu"}},"xrefs":[{"source":"MONDO","code":"18719","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681120","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":211247,"name":"Rare capillary malformation","classifications":[147,198]},{"orpha":459526,"name":"Rare genetic capillary malformation","classifications":[156]}],"children":[{"orpha":276280,"name":"Hemihyperplasia-multiple lipomatosis syndrome","type":"Malformation syndrome"},{"orpha":60040,"name":"Megalencephaly-capillary malformation-polymicrogyria syndrome","type":"Malformation syndrome"},{"orpha":2703,"name":"Port-wine nevi-mega cisterna magna-hydrocephalus syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}