Term Name:	muscular dystrophy-dystroglycanopathy type B15
Synonyms:	congenital muscular dystrophy DPM3-related, MDDGB15
Definition:	A muscular dystrophy-dystroglycanopathy type B that has_material_basis_in homozygous or compound heterozygous mutation in the DPM3 gene on chromosome 1q22.
Ontology:	Human Disease [DOID:0112376]   ( DOID:0112376 )