Term Name:	autosomal recessive limb-girdle muscular dystrophy type 2C
Synonyms:	autosomal recessive Duchenne-like muscular dystrophy type 1, deficiency of sarcoglycan gamma, DMDA1, gamma-sarcoglycanopathy, LGMD2C, limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency, Maghrebian myopathy, muscular dystrophy, limb-girdle, type 2C, SCARMD, severe childhood autosomal recessive muscular dystrophy North African type
Definition:	An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12.
Ontology:	Human Disease [DOID:0110277]   ( DOID:0110277 )