{"orpha":102006,"name":"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-102006/","orphanet_url":"https://www.orpha.net/en/disease/detail/102006","names":{"fr":{"name":"Malformation neurovasculaire"},"de":{"name":"Neurovaskuläre Fehlbildung","synonyms":["Neurovaskuläre Malformation"]},"es":{"name":"Malformación neurovascular"},"it":{"name":"Malformazione neurovascolare"},"nl":{"name":"Neurovasculaire malformatie"},"pt":{"name":"Malformação neurovascular"},"pl":{"name":"Malformacja nerwowo-naczyniowa"},"cs":{"name":"Neurovaskulární malformace"},"uk":{"name":"Нервово-судинні вади розвитку"},"zh":{"name":"神经血管畸形"},"tr":{"name":"Nörovasküler malformasyon"}},"xrefs":[{"source":"MONDO","code":"15145","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681774","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19819","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":71281,"name":"Rare central nervous system and retinal vascular disease","classifications":[181]}],"children":[{"orpha":723432,"name":"Central nervous system venous vascular malformation","type":"Clinical group"},{"orpha":353334,"name":"Congenital retinal arteriovenous communication","type":"Morphological anomaly"},{"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":981,"name":"Internal carotid absence","type":"Morphological anomaly"},{"orpha":715750,"name":"Intracranial fast-flow vascular malformation","type":"Clinical group"},{"orpha":715757,"name":"Metameric fast-flow vascular malformation","type":"Clinical group"},{"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":715025,"name":"Spinal fast-flow vascular malformation","type":"Clinical group"},{"orpha":3205,"name":"Sturge-Weber syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["All ages"],"prevalence":[],"phenotypes":null}