{"orpha":477771,"name":"Rare disorder with a moyamoya angiopathy","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-477771/","orphanet_url":"https://www.orpha.net/en/disease/detail/477771","names":{"fr":{"name":"Maladie rare avec angiopathie de Moyamoya"},"de":{"name":"Seltene Krankheit mit Moyamoya-Angiopathie"},"es":{"name":"Trastorno raro con angiopatía de moyamoya"},"it":{"name":"Malattia rara con agiopatia di moyamoya"},"nl":{"name":"Zeldzame stoornis met een moyamoya-angiopathie"},"pt":{"name":"Doença rara com angiopatia de Moyamoya"},"pl":{"name":"Zespół Moyamoya"},"cs":{"name":"Vzácné onemocnění s moyamoya angiopatií"},"uk":{"name":"Рідкісне захворювання з ангіопатією Моямоя"},"zh":{"name":"罕见病合并烟雾病"},"tr":{"name":"Moyamoya anjiyopatisi ile seyreden nadir bozukluk"}},"xrefs":[{"source":"MONDO","code":"18792","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681260","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":183503,"name":"Genetic central nervous system and retinal vascular disease","classifications":[156]},{"orpha":477768,"name":"Moyamoya angiopathy","classifications":[181]}],"children":[{"orpha":51,"name":"Aicardi-Goutières syndrome","type":"Disease"},{"orpha":3071,"name":"Costello syndrome","type":"Malformation syndrome"},{"orpha":870,"name":"Down syndrome","type":"Malformation syndrome"},{"orpha":481662,"name":"Familial Chilblain lupus","type":"Disease"},{"orpha":2637,"name":"Microcephalic osteodysplastic primordial dwarfism type II","type":"Malformation syndrome"},{"orpha":280679,"name":"Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome","type":"Disease"},{"orpha":401945,"name":"Moyamoya disease with early-onset achalasia","type":"Disease"},{"orpha":636,"name":"Neurofibromatosis type 1","type":"Disease"},{"orpha":648,"name":"Noonan syndrome","type":"Malformation syndrome"},{"orpha":363972,"name":"Noonan syndrome-like disorder with juvenile myelomonocytic leukemia","type":"Malformation syndrome"},{"orpha":42775,"name":"PHACE syndrome","type":"Malformation syndrome"},{"orpha":232,"name":"Sickle cell anemia","type":"Disease"},{"orpha":881,"name":"Turner syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}