{"orpha":101151,"name":"Dystonia 14","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["DYT14"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal dominant dopa-responsive dystonia","url":"https://raremap.alftech.space/d/ORPHA-101151/","orphanet_url":"https://www.orpha.net/en/disease/detail/101151","names":{"fr":{"name":"Dystonie 14","synonyms":["DYT14"]},"de":{"name":"Dystonie 14","synonyms":["DYT14"]},"es":{"name":"Distonía 14"},"it":{"name":"Distonia 14 (DYT14)"},"nl":{"name":"Dystonie 14","synonyms":["DYT14"]},"pt":{"name":"Distonia 14"},"pl":{"name":"Dystonia 14","synonyms":["DYT14"]},"cs":{"name":"Dystonie 14","synonyms":["DYT14"]},"uk":{"name":"Дистонія 14","synonyms":["DYT14"]},"zh":{"name":"肌张力障碍14型","synonyms":["肌张力障碍14"]},"tr":{"name":"Distoni 14","synonyms":["DYT14"]}},"xrefs":[],"associations":[{"type":"Moved to","orpha":98808,"name":"Autosomal dominant dopa-responsive dystonia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}