{"orpha":71281,"name":"Rare central nervous system and retinal 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-71281/","orphanet_url":"https://www.orpha.net/en/disease/detail/71281","names":{"fr":{"name":"Maladie vasculaire rare du système nerveux central et de la rétine"},"de":{"name":"ZNS- und Netzhautkrankheit, vaskuläre seltene"},"es":{"name":"Enfermedad rara del sistema nervioso central y vascular de la retina"},"it":{"name":"Malattia rara vascolare retinica e del sistema nervoso centrale"},"nl":{"name":"Zeldzame vasculaire aandoening van centraal zenuwstelsel en retina"},"pt":{"name":"Doença vascular do sistema nervoso central e da retina, rara"},"pl":{"name":"Rzadka choroba centralnego układu nerwowego i choroba naczyniowa siatkówki"},"cs":{"name":"Vzácná porucha centrálního nervového systému a cévní choroba sítnice"},"uk":{"name":"Рідкісні захворювання центральної нервової системи та судин сітківки"},"zh":{"name":"罕见中枢神经系统和视网膜血管疾病"},"tr":{"name":"Nadir merkezi sinir sistemi ve retinal damar hastalığı"}},"xrefs":[{"source":"MONDO","code":"19110","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681266","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":98006,"name":"Rare neurologic disease","classifications":[181]}],"children":[{"orpha":90065,"name":"Acquired aneurysmal subarachnoid hemorrhage","type":"Particular clinical situation in a disease or syndrome"},{"orpha":329217,"name":"Cerebral sinovenous thrombosis","type":"Disease"},{"orpha":447788,"name":"Cerebral visual impairment","type":"Clinical syndrome"},{"orpha":190,"name":"Coats disease","type":"Disease"},{"orpha":891,"name":"Familial exudative vitreoretinopathy","type":"Disease"},{"orpha":569,"name":"Familial or sporadic hemiplegic migraine","type":"Disease"},{"orpha":284247,"name":"Familial retinal arterial macroaneurysm","type":"Malformation syndrome"},{"orpha":477754,"name":"Genetic cerebral small vessel disease","type":"Category"},{"orpha":209943,"name":"IRVAN syndrome","type":"Disease"},{"orpha":689001,"name":"Isolated spontaneous cervical artery dissection","type":"Disease"},{"orpha":477768,"name":"Moyamoya angiopathy","type":"Clinical group"},{"orpha":404463,"name":"Multisystemic smooth muscle dysfunction syndrome","type":"Disease"},{"orpha":137577,"name":"Neonatal hypoxic and ischemic brain injury","type":"Particular clinical situation in a disease or syndrome"},{"orpha":102006,"name":"Neurovascular malformation","type":"Category"},{"orpha":439175,"name":"Pediatric arterial ischemic stroke","type":"Clinical syndrome"},{"orpha":140989,"name":"Primary angiitis of the central nervous system","type":"Disease"},{"orpha":758,"name":"Pseudoxanthoma elasticum","type":"Disease"},{"orpha":482092,"name":"Rare idiopathic macular telangiectasia","type":"Category"},{"orpha":820,"name":"Sneddon syndrome","type":"Disease"},{"orpha":838,"name":"Susac syndrome","type":"Disease"},{"orpha":353356,"name":"Vasoproliferative tumor of the retina","type":"Disease"},{"orpha":892,"name":"Von Hippel-Lindau disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}