{"orpha":264,"name":"Autosomal dominant limb-girdle muscular dystrophy type 1B","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["LGMD1B","Limb-girdle muscular dystrophy due to lamin A/C deficiency"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal dominant Emery-Dreifuss muscular dystrophy","url":"https://raremap.alftech.space/d/ORPHA-264/","orphanet_url":"https://www.orpha.net/en/disease/detail/264","names":{"fr":{"name":"Dystrophie musculaire des ceintures autosomique dominante type 1B","synonyms":["Dystrophie musculaire des ceintures par déficit en lamine A/C","LGMD1B"]},"de":{"name":"Gliedergürtelmuskeldystrophie, autosomal-dominante, Typ 1B","synonyms":["Gliedergürtelmuskeldystrophie durch Lamin A/C -Mangel","LGMD1B"]},"es":{"name":"Distrofia muscular de cinturas autosómica dominante tipo 1B","synonyms":["Distrofia muscular de cinturas por deficiencia de lamina A/C","LGMD1B"]},"it":{"name":"Distrofia muscolare dei cingoli, autosomica dominante, tipo 1B","synonyms":["Distrofia muscolare dei cingoli da deficit di lamina A/C","LGMD1B"]},"nl":{"name":"Autosomaal dominante limb-girdle-spierdystrofie type 1B","synonyms":["Autosomaal dominante ledemaatgordel-spierdystrofie type 1B","LGMD1B","Limb-girdle-spierdystrofie door lamine A/C-deficiëntie","Autosomaal dominante bekken- en schoudergordel-spierdystrofie type 1B"]},"pt":{"name":"Distrofia muscular das cinturas dos membros autossómica dominante tipo 1B","synonyms":["Distrofia muscular das cinturas dos membros por deficiência de lamina A/C"]},"pl":{"name":"Autosomalna recesywna dystrofia obręczowo-kończynowa typu 1B","synonyms":["Dystrofia obręczowo-kończynowa z powodu niedoboru laminy A/C","LGMD1B"]},"cs":{"name":"Autozomálně dominantní pletencová svalová dystrofie, typ 1B","synonyms":["LGMD1B","Pletencová svalová dystrofie způsobená deficitem laminu A/C"]},"uk":{"name":"Аутосомно-домінантна мязова дистрофія скелетних мязів кінцівок, тип 1B","synonyms":["LGMD1B","Мязова дистрофія мязів поясу кінцівок внаслідок дефіциту ламіну А/С"]},"zh":{"name":"1B型常染色体显性遗传肢带肌营养不良","synonyms":["LGMD1B"]},"tr":{"name":"Otozomal dominant ekstremite kavşak tip kas distrofisi tip 1B","synonyms":["Lamin A / C eksikliğine bağlı ekstremite-kavşak tipi kas distrofisi","LGMD1B"]}},"xrefs":[{"source":"UMLS","code":"C1834653","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":98853,"name":"Autosomal dominant Emery-Dreifuss muscular dystrophy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}