Term Name: congenital muscular dystrophy-dystroglycanopathy type A9
Synonyms: congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9, MDDGA9, Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
Definition: A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.
Ontology: Human Disease [DOID:0111232]   ( DOID:0111232 )

Relationships
is a type of: congenital muscular dystrophy-dystroglycanopathy type A