{"orpha":494457,"name":"Rare hyperkinetic movement disorder","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-494457/","orphanet_url":"https://www.orpha.net/en/disease/detail/494457","names":{"fr":{"name":"Trouble du mouvement hyperkinétique rare"},"de":{"name":"Seltene Form der hyperkinetischen Bewegungsstörung"},"es":{"name":"Trastorno raro del movimiento hipercinético"},"it":{"name":"Disturbo ipercinetico raro del movimento"},"nl":{"name":"Zeldzame hyperkinetische bewegingsstoornis"},"pt":{"name":"Doença do movimento hipercinético raro"},"pl":{"name":"Rzadkie zaburzenie hiperkinetyczne ruchu"},"cs":{"name":"Vzácná hyperkinetická pohybová porucha"},"uk":{"name":"Рідкісний гіперкінетичний руховий розлад"},"zh":{"name":"罕见多动障碍"},"tr":{"name":"Nadir hiperkinetik hareket bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681221","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":102003,"name":"Rare movement disorder","classifications":[181]}],"children":[{"orpha":592564,"name":"GNAO1-related developmental delay-seizures-movement disorder spectrum","type":"Disease"},{"orpha":522077,"name":"Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome","type":"Disease"},{"orpha":306765,"name":"Motor stereotypies","type":"Category"},{"orpha":684240,"name":"Neurodevelopmental disorder-spasticity-movement disorder-epileptic syndrome","type":"Malformation syndrome"},{"orpha":306715,"name":"Rare choreic movement disorder","type":"Category"},{"orpha":68363,"name":"Rare dystonia","type":"Category"},{"orpha":306747,"name":"Rare myoclonus","type":"Category"},{"orpha":306712,"name":"Rare tremor disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}