{"orpha":371436,"name":"Genetic neurovascular 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-371436/","orphanet_url":"https://www.orpha.net/en/disease/detail/371436","names":{"fr":{"name":"Malformation neurovasculaire d'origine génétique"},"de":{"name":"Neurovaskuläre Fehlbildung, genetisch bedingte"},"es":{"name":"Malformación neurovascular genética"},"it":{"name":"Malformazione neurovascolare genetica"},"nl":{"name":"Genetische neurovasculaire malformatie"},"pt":{"name":"Malformação neurovascular genética"},"pl":{"name":"Malformacja nerwowo-naczyniowa uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněné neurovaskulární malformace"},"uk":{"name":"Генетично обумовлена нейросудинна вада розвитку"},"zh":{"name":"遗传性神经血管畸形"},"tr":{"name":"Genetik nörovasküler malformasyon"}},"xrefs":[{"source":"UMLS","code":"C5681150","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183503,"name":"Genetic central nervous system and retinal vascular disease","classifications":[156]}],"children":[{"orpha":46724,"name":"Brain arteriovenous malformation, nidus type","type":"Morphological anomaly"},{"orpha":221061,"name":"Familial cerebral cavernous malformation","type":"Malformation syndrome"},{"orpha":231160,"name":"Familial cerebral saccular aneurysm","type":"Disease"},{"orpha":83454,"name":"Glomuvenous malformation","type":"Malformation syndrome"},{"orpha":774,"name":"Hereditary hemorrhagic telangiectasia","type":"Disease"},{"orpha":1062,"name":"Hereditary neurocutaneous malformation","type":"Disease"},{"orpha":521445,"name":"Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome","type":"Malformation syndrome"},{"orpha":42775,"name":"PHACE syndrome","type":"Malformation syndrome"},{"orpha":71213,"name":"Retinal cavernous hemangioma","type":"Disease"},{"orpha":1053,"name":"Vein of Galen malformation","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}