{"orpha":233655,"name":"Rare genetic vascular disease","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-233655/","orphanet_url":"https://www.orpha.net/en/disease/detail/233655","names":{"fr":{"name":"Maladie vasculaire génétique rare"},"de":{"name":"Gefäßkrankheit, seltene, genetisch bedingte"},"es":{"name":"Enfermedades vasculares genéticas raras"},"it":{"name":"Malattia vascolare genetica rara"},"nl":{"name":"Zeldzame genetische vasculaire ziekte"},"pt":{"name":"Doença vascular genética rara"},"pl":{"name":"Rzadka choroba naczyniowa uwarunkowana genetycznie"},"cs":{"name":"Vzácné genetické vaskulární onemocnění"},"uk":{"name":"Рідкісне генетично обумовлене захворювання судин"},"zh":{"name":"罕见遗传性血管疾病"},"tr":{"name":"Nadir genetik vasküler hastalık"}},"xrefs":[{"source":"MONDO","code":"16517","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680923","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98028,"name":"Rare circulatory system disease"},"parents":[{"orpha":496924,"name":"Non-inflammatory vasculopathy","classifications":[198]},{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":90349,"name":"Autosomal recessive cutis laxa type 1","type":"Disease"},{"orpha":404553,"name":"Deficiency of adenosine deaminase 2","type":"Disease"},{"orpha":86,"name":"Familial abdominal aortic aneurysm","type":"Disease"},{"orpha":51608,"name":"Generalized arterial calcification of infancy","type":"Disease"},{"orpha":289601,"name":"Hereditary arterial and articular multiple calcification syndrome","type":"Disease"},{"orpha":314718,"name":"Lethal arteriopathy syndrome due to fibulin-4 deficiency","type":"Disease"},{"orpha":285014,"name":"Rare disease with thoracic aortic aneurysm and aortic dissection","type":"Category"},{"orpha":425120,"name":"STING-associated vasculopathy with onset in infancy","type":"Disease"},{"orpha":820,"name":"Sneddon syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}