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 )

Relationships
is a type of: autosomal recessive disease muscular dystrophy-dystroglycanopathy type B