{"orpha":496916,"name":"Rare genetic 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-496916/","orphanet_url":"https://www.orpha.net/en/disease/detail/496916","names":{"fr":{"name":"Trouble du mouvement hyperkinétique génétique rare"},"de":{"name":"Seltene genetische hyperkinetische Bewegungsstörung"},"es":{"name":"Trastorno raro genético del movimiento hipercinético"},"it":{"name":"Malattia genetica rara da movimenti ipercinetici"},"nl":{"name":"Zeldzame genetische hyperkinetische bewegingsstoornis"},"pt":{"name":"Doença do movimento hipercinético genético raro"},"pl":{"name":"Rzadkie genetyczne zaburzenie ruchu hiperkinetycznego"},"cs":{"name":"Vzácná geneticky podmíněná hyperkinetická porucha"},"uk":{"name":"Рідкісний генетично обумовлений гіперкінетичний руховий розлад"},"zh":{"name":"罕见遗传性运动亢进症"},"tr":{"name":"Nadir genetik hiperkinetik hareket bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681226","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":183521,"name":"Rare genetic movement disorder","classifications":[156]}],"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":306719,"name":"Neurodegenerative disease with chorea","type":"Category"},{"orpha":684240,"name":"Neurodevelopmental disorder-spasticity-movement disorder-epileptic syndrome","type":"Malformation syndrome"},{"orpha":391799,"name":"Rare genetic dystonia","type":"Category"},{"orpha":307064,"name":"Rare genetic myoclonus","type":"Category"},{"orpha":307061,"name":"Rare genetic tremor disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}