{"orpha":183521,"name":"Rare genetic 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-183521/","orphanet_url":"https://www.orpha.net/en/disease/detail/183521","names":{"fr":{"name":"Anomalie du mouvement rare de cause génétique"},"de":{"name":"Bewegungsstörung, genetisch bedingte, seltene"},"es":{"name":"Trastorno raro del movimiento de origen genético"},"it":{"name":"Disturbo genetico raro del movimento"},"nl":{"name":"Zeldzame genetische bewegingsstoornis"},"pt":{"name":"Doença do movimento, genética, raro"},"pl":{"name":"Rzadkie zaburzenia ruchu uwarunkowane genetycznie"},"cs":{"name":"Vzácné geneticky podmíněné poruchy hybnosti"},"uk":{"name":"Рідкісне генетично обумовлене порушення руху"},"zh":{"name":"罕见遗传性运动障碍"},"tr":{"name":"Nadir genetik hareket bozukluğu"}},"xrefs":[{"source":"MONDO","code":"15957","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680562","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":238722,"name":"Familial congenital mirror movements","type":"Disease"},{"orpha":3197,"name":"Hereditary hyperekplexia","type":"Disease"},{"orpha":163985,"name":"Hyperekplexia-epilepsy syndrome","type":"Disease"},{"orpha":369847,"name":"Intellectual disability-hyperkinetic movement-truncal ataxia syndrome","type":"Disease"},{"orpha":307058,"name":"Miscellaneous movement disorder due to genetic neurodegenerative disease","type":"Category"},{"orpha":496916,"name":"Rare genetic hyperkinetic movement disorder","type":"Category"},{"orpha":307052,"name":"Rare genetic parkinsonian disorder","type":"Category"},{"orpha":306768,"name":"Rare paroxysmal movement disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}