{"orpha":306765,"name":"Motor stereotypies","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-306765/","orphanet_url":"https://www.orpha.net/en/disease/detail/306765","names":{"fr":{"name":"Stéréotypies motrices"},"de":{"name":"Bewegungsstörung, stereotype"},"es":{"name":"Estereotipias motoras"},"it":{"name":"Stereotipie motorie"},"nl":{"name":"Motorische stereotypieën"},"pt":{"name":"Estereotipias motoras"},"pl":{"name":"Stereotypie ruchowe"},"cs":{"name":"Motorické stereotypie"},"uk":{"name":"Рухові стереотипії"},"zh":{"name":"刻板运动"},"tr":{"name":"Motor stereotipleri"}},"xrefs":[{"source":"MONDO","code":"17656","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D013239","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":496916,"name":"Rare genetic hyperkinetic movement disorder","classifications":[156]},{"orpha":494457,"name":"Rare hyperkinetic movement disorder","classifications":[181]}],"children":[{"orpha":3095,"name":"Atypical Rett syndrome","type":"Disease"},{"orpha":505652,"name":"CDKL5-deficiency disorder","type":"Disease"},{"orpha":561854,"name":"FOXG1 syndrome","type":"Disease"},{"orpha":908,"name":"Fragile X syndrome","type":"Malformation syndrome"},{"orpha":778,"name":"Rett syndrome","type":"Disease"},{"orpha":904,"name":"Williams syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}