ORPHA:466801

OBSOLETE: LIMS2-related myopathy

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Progressive muscular dystrophy

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: LIMS2-related myopathy
fr	OBSOLETE : Myopathie associée à LIMS2
de	OBSOLET: Gliedergürtelmuskeldystrophie, autosomal-rezessive, Typ 2W	OBSOLET: LGMD2W
es	OBSOLETO: Distrofia muscular de cinturas autosómica recesiva tipo 2W	OBSOLETO: LGMD2W
it	OBSOLETO: Distrofia muscolare dei cingoli automica recessiva tipo 2W
nl	OBSOLEET: Autosomaal recessieve limb-girdle-spierdystrofie type 2W	OBSOLEET: Autosomaal recessieve bekken- en schoudergordel-spierdystrofie type 2W · OBSOLEET: Autosomaal recessieve ledemaatgordel-spierdystrofie type 2W · OBSOLEET: LGMD2W
pt	OBSOLETO: Distrofia muscular de cinturas dos membros LIMS2-relacionada	OBSOLETO: Distrofia muscular de cinturas autossómica recessiva tipo 2W
pl	NIEAKTUALNE: Autosomalna recesywna dystrofia obręczowo-kończynowa typu 2W	NIEAKTUALNE: LGMD2W
cs	NEAKTUÁLNÍ: LIMS2-asociovaná svalová dystrofie pletencového typu	NEAKTUÁLNÍ: LGMD2W
uk	ЗАСТАРІЛО: Міопатія, повязана з LIMS2
zh	LIMS2相关的肢带肌营养不良症	常染色体隐性肢带肌营养不良2W型
tr	LIMS2-ilişkili ekstremite kavşak tip kas distrofisi	LGMD2W · LGMD tip 2W · LIMS2-ilişkili LGM · Ekstremite-kavşak tipi kas distrofisi tip 2W · Otozomal çekinik ekstremite-kavşak tipi kas distrofisi tip 2W

Definition in:

qualifier = Orphanet mapping relation

No cross-references in this release.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.