{"orpha":306759,"name":"Non progressive epilepsy and/or ataxia with myoclonus as a major feature","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-306759/","orphanet_url":"https://www.orpha.net/en/disease/detail/306759","names":{"fr":{"name":"Epilepsie et/ou ataxie non progressive avec myoclonie comme manifestation majeure"},"de":{"name":"Nicht-progressive Epilepsie und/oder Ataxie mit Myoklonie als Hauptmerkmal"},"es":{"name":"Epilepsia no progresiva y/o ataxia con mioclonos como característica principal"},"it":{"name":"Epilessia non progressiva e/o atassia con mioclono come segno cardinale"},"nl":{"name":"Niet-progressieve epilepsie en/of ataxie met myoclonus als hoofdkenmerk"},"pt":{"name":"Epilepsia não progressiva e/ou ataxia com mioclonia como característica principal"},"pl":{"name":"Niepostępująca padaczka i(lub) ataksja, w której mioklonus jest objawem głównym"},"cs":{"name":"Non-progresivní epilepsie a/nebo ataxie s myoklonem jako hlavním příznakem"},"uk":{"name":"Непрогресуюча епілепсія та/або атаксія з міоклонусом як основною ознакою"},"zh":{"name":"肌阵挛为主的非进行性癫痫和/或共济失调"},"tr":{"name":"Esas klinik özelliği miyoklonus olan ilerleyici olmayan epilepsi ve/veya ataksi"}},"xrefs":[{"source":"MONDO","code":"17654","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681051","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":306756,"name":"Epilepsy and/or ataxia with myoclonus as a major feature","classifications":[156,181]}],"children":[{"orpha":86911,"name":"Epilepsy with myoclonic absences","type":"Disease"},{"orpha":307,"name":"Juvenile myoclonic epilepsy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}