{"orpha":221106,"name":"OBSOLETE: Isolated facial myokymia","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Acquired peripheral movement disorder","url":"https://raremap.alftech.space/d/ORPHA-221106/","orphanet_url":"https://www.orpha.net/en/disease/detail/221106","names":{"fr":{"name":"OBSOLETE : Myokymie faciale isolée"},"de":{"name":"OBSOLET: Myokymie, isolierte, des Gesichts"},"es":{"name":"OBSOLETO: Mioquimia facial aislada"},"it":{"name":"OBSOLETO: Miochimia facciale isolata"},"nl":{"name":"OBSOLEET: Geïsoleerde faciale myokymie"},"pt":{"name":"OBSOLETO: Mioquimia isolada da face"},"pl":{"name":"NIEAKTUALNE: Izolowana miokimia twarzowa"},"cs":{"name":"NEAKTUÁLNÍ: Izolovaná faciální myokymie"},"uk":{"name":"ЗАСТАРІЛО: Ізольована міокімія обличчя"},"zh":{"name":"孤立性面肌纤维颤搐"},"tr":{"name":"İzole fasiyal miyokimi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":221114,"name":"Acquired peripheral movement disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}