{"orpha":459526,"name":"Rare genetic capillary malformation","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-459526/","orphanet_url":"https://www.orpha.net/en/disease/detail/459526","names":{"fr":{"name":"Malformation capillaire génétique rare"},"de":{"name":"Seltene genetische kapilläre Fehlbildung"},"es":{"name":"Malformación capilar genética rara"},"it":{"name":"Malformazione capillare genetica rara"},"nl":{"name":"Zeldzame genetische capillaire malformatie"},"pt":{"name":"Malformação capilar genética rara"},"pl":{"name":"Rzadka genetycznie uwarunkowana malformacja naczyniowa"},"cs":{"name":"Vzácné geneticky podmíněné kapilární malformace"},"uk":{"name":"Рідкісна генетично обумовлена капілярна вада розвитку"},"zh":{"name":"遗传性罕见毛细血管畸形"},"tr":{"name":"Nadir genetik kılcal damar malformasyonu"}},"xrefs":[{"source":"MONDO","code":"18728","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681109","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":211240,"name":"Genetic vascular anomaly","classifications":[156]}],"children":[{"orpha":624,"name":"Familial multiple nevi flammei","type":"Morphological anomaly"},{"orpha":774,"name":"Hereditary hemorrhagic telangiectasia","type":"Disease"},{"orpha":458830,"name":"Rare capillary malformation with associated anomalies","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}