{"orpha":98688,"name":"Oculomotor apraxia","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-98688/","orphanet_url":"https://www.orpha.net/en/disease/detail/98688","names":{"fr":{"name":"Apraxie oculomotrice"},"de":{"name":"Okulomotorische Apraxie"},"es":{"name":"Apraxia oculomotora y enfermedades oculomotoras relacionadas"},"it":{"name":"Aprassia oculomotoria e malattie oculomotorie associate"},"nl":{"name":"Oculomotorische apraxie"},"pt":{"name":"Apraxia oculomotora e doenças oculomotora relacionada"},"pl":{"name":"Apraksja okoruchowa związana z choroba okoruchową"},"cs":{"name":"Apraxie okohybných svalů nebo příbuzná onemocnění"},"uk":{"name":"Окуломоторна апраксія"},"zh":{"name":"动眼运动异常"},"tr":{"name":"Okülomotor apraksi"}},"xrefs":[{"source":"ICD-11","code":"9C82.4","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"855225863"},{"source":"UMLS","code":"C3489733","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":522508,"name":"Rare genetic ophthalmic disorder with cortical involvement","classifications":[156]},{"orpha":519343,"name":"Rare ophthalmic disorder with cortical involvement","classifications":[189]}],"children":[{"orpha":370022,"name":"Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome","type":"Disease"},{"orpha":459033,"name":"Ataxia-oculomotor apraxia type 4","type":"Disease"},{"orpha":77261,"name":"Gaucher disease type 3","type":"Clinical subtype"},{"orpha":2072,"name":"Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome","type":"Clinical subtype"},{"orpha":1125,"name":"Ocular motor apraxia, Cogan type","type":"Disease"},{"orpha":505242,"name":"Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}