Human genes for autosomal recessive limb-girdle muscular dystrophy type 2D
Autosomal recessive limb-girdle muscular dystrophy type 2D [DOID:0110278]
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.
Synonyms: autosomal recessive limb-girdle muscular dystrophy type 2D, autosomal recessive limbgirdle muscular dystrophy type 2D, DOID:0110278, Alpha-sarcoglycanopathy, DMDA2 ...