Term Name:	congenital muscular dystrophy-dystroglycanopathy type A13
Synonyms:	congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13, MDDGA13, Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related, Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
Definition:	A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in B4GAT1 on 11q13.2.
Ontology:	Human Disease [DOID:0111238]   ( DOID:0111238 )