Term Name:	autosomal recessive limb-girdle muscular dystrophy type 2P
Synonyms:	LGMD2P, MDDGC9, muscular dystrophy-dystroglycanopathy (limb-girdle) type C9, muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
Definition:	An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding alpha-dystroglycan (DAG1) on chromosome 3p21.
Ontology:	Human Disease [DOID:0110293]   ( DOID:0110293 )