Term Name:	autosomal recessive limb-girdle muscular dystrophy type 2D
Synonyms:	Alpha-sarcoglycanopathy, DMDA2, Duchenne-like autosomal recessive muscular dystrophy type 2, LGMD2D, muscular dystrophy, limb-girdle, type 2D, primary adhalinopathy
Definition:	An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the alpha-sarcoglycan gene (SGCA) on chromosome 17q.
Ontology:	Human Disease [DOID:0110278]   ( DOID:0110278 )