{"orpha":1155,"name":"OBSOLETE: Arthrogryposis due to muscular dystrophy","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 Arthrogryposis multiplex congenita","url":"https://raremap.alftech.space/d/ORPHA-1155/","orphanet_url":"https://www.orpha.net/en/disease/detail/1155","names":{"fr":{"name":"OBSOLETE : Arthrogrypose par dystrophie musculaire"},"de":{"name":"OBSOLET: Arthrogrypose infolge Muskeldystrophie"},"es":{"name":"OBSOLETO: Artrogriposis por distrofia muscular"},"it":{"name":"OBSOLETO: Artrogriposi da distrofia muscolare"},"nl":{"name":"OBSOLEET: Artrogrypose als gevolg van spierdystrofie"},"pt":{"name":"OBSOLETO: Artrogripose por distrofia muscular"},"pl":{"name":"NIEAKTUALNE: Artogrypoza spowodowana dystrofia miesni"},"cs":{"name":"NEAKTUÁLNÍ: Artrogrypóza způsobená svalovou dystrofií"},"uk":{"name":"ЗАСТАРІЛО: Артрогрипоз внаслідок мязової дистрофії"},"zh":{"name":"弃用：肌营养不良症所致关节挛缩"},"tr":{"name":"Eski adı: Kas distrofisine bağlı artrogripozis"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":1037,"name":"Arthrogryposis multiplex congenita"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}