Term Name: | congenital muscular dystrophy-dystroglycanopathy type A9 |
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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 ) |