{"orpha":183503,"name":"Genetic 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-183503/","orphanet_url":"https://www.orpha.net/en/disease/detail/183503","names":{"fr":{"name":"Maladie vasculaire du système nerveux central et de la rétine de cause génétique"},"de":{"name":"ZNS-Fehlbildung und vaskuläre Netzhautkrankheit, genetisch bedingt"},"es":{"name":"Enfermedad vascular del sistema nervioso central y de la retina de origen genético."},"it":{"name":"Malattia vascolare del sistema nervoso centrale e della retina di origine genetica"},"nl":{"name":"Genetische centraal zenuwstelsel en retinale vasculaire ziekte"},"pt":{"name":"Doença genética do sistema nervoso central e vascular retiniana"},"pl":{"name":"Choroba centralnego układu nerwowego i naczyń siatkówki uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněná onemocnění cév centrálního nervového systému a sítnice"},"uk":{"name":"Генетично обумовлене захворювання центральної нервової системи та судин сітківки"},"zh":{"name":"遗传性中枢神经系统和视网膜血管病"},"tr":{"name":"Genetik merkezi sinir sistemi ve retina damar hastalığı"}},"xrefs":[{"source":"MONDO","code":"15953","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681839","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":71859,"name":"Rare genetic neurological disorder","classifications":[156]}],"children":[{"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":371436,"name":"Genetic neurovascular malformation","type":"Category"},{"orpha":689001,"name":"Isolated spontaneous cervical artery dissection","type":"Disease"},{"orpha":404463,"name":"Multisystemic smooth muscle dysfunction syndrome","type":"Disease"},{"orpha":140989,"name":"Primary angiitis of the central nervous system","type":"Disease"},{"orpha":758,"name":"Pseudoxanthoma elasticum","type":"Disease"},{"orpha":477771,"name":"Rare disorder with a moyamoya angiopathy","type":"Category"},{"orpha":892,"name":"Von Hippel-Lindau disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}