{"orpha":466801,"name":"OBSOLETE: LIMS2-related myopathy","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 Progressive muscular dystrophy","url":"https://raremap.alftech.space/d/ORPHA-466801/","orphanet_url":"https://www.orpha.net/en/disease/detail/466801","names":{"fr":{"name":"OBSOLETE : Myopathie associée à LIMS2"},"de":{"name":"OBSOLET: Gliedergürtelmuskeldystrophie, autosomal-rezessive, Typ 2W","synonyms":["OBSOLET: LGMD2W"]},"es":{"name":"OBSOLETO: Distrofia muscular de cinturas autosómica recesiva tipo 2W","synonyms":["OBSOLETO: LGMD2W"]},"it":{"name":"OBSOLETO: Distrofia muscolare dei cingoli automica recessiva tipo 2W"},"nl":{"name":"OBSOLEET: Autosomaal recessieve limb-girdle-spierdystrofie type 2W","synonyms":["OBSOLEET: Autosomaal recessieve bekken- en schoudergordel-spierdystrofie type 2W","OBSOLEET: Autosomaal recessieve ledemaatgordel-spierdystrofie type 2W","OBSOLEET: LGMD2W"]},"pt":{"name":"OBSOLETO: Distrofia muscular de cinturas dos membros LIMS2-relacionada","synonyms":["OBSOLETO: Distrofia muscular de cinturas autossómica recessiva tipo 2W"]},"pl":{"name":"NIEAKTUALNE: Autosomalna recesywna dystrofia obręczowo-kończynowa typu 2W","synonyms":["NIEAKTUALNE: LGMD2W"]},"cs":{"name":"NEAKTUÁLNÍ: LIMS2-asociovaná svalová dystrofie pletencového typu","synonyms":["NEAKTUÁLNÍ: LGMD2W"]},"uk":{"name":"ЗАСТАРІЛО: Міопатія, повязана з LIMS2"},"zh":{"name":"LIMS2相关的肢带肌营养不良症","synonyms":["常染色体隐性肢带肌营养不良2W型"],"definition":"是常染色体隐性肢带型肌营养不良症的一种亚型，其特点是儿童起病，上、下肢近端骨骼肌严重、进行性萎缩，以后累及远端肌肉，出现严重的四肢瘫痪、小腿肥大、三角舌和扩张性心肌病。骨骼肌发生弥漫性、双侧性、对称性严重萎缩，并有脂肪浸润。"},"tr":{"name":"LIMS2-ilişkili ekstremite kavşak tip kas distrofisi","synonyms":["LGMD2W","LGMD tip 2W","LIMS2-ilişkili LGM","Ekstremite-kavşak tipi kas distrofisi tip 2W","Otozomal çekinik ekstremite-kavşak tipi kas distrofisi tip 2W"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":206644,"name":"Progressive muscular dystrophy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}