Term Name:	muscular dystrophy-dystroglycanopathy type B1
Synonyms:	CMD due to dystroglycanopathy
Definition:	A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase.
Ontology:	Human Disease [DOID:0050588]   (DOID:0050588)