Category:Calpainopathy

**autosomal recessive limb-girdle muscular dystrophy type 2A**
	autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15
	Upload media
	Wikipedia
Instance of	rare disease; class of disease;
Subclass of	autosomal recessive limb-girdle muscular dystrophy; disease;
Authority file
	Q17177467;
	Reasonator; Scholia; Wikidocumentaries; PetScan; statistics; WikiMap; Locator tool; KML file; Search depicted;

Subcategories

This category has only the following subcategory.

This category contains only the following file.