congenital muscular dystrophy-dystroglycanopathy type A10 (DOID:0111239)
Alliance: disease page
Synonyms: congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10; MDDGA10; Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related
Alt IDs: OMIM:615041
Definition: A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2.