congenital muscular dystrophy-dystroglycanopathy type A9 (DOID:0111232)
Alliance: disease page
Synonyms: congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9; MDDGA9; Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
Alt IDs: OMIM:616538
Definition: A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.