muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7 (Monarch Disease Ontology term MONDO_0013835) is any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the ISPD gene. Also known as: ISPD muscular dystrophy-dystroglycanopathy, type A, Walker-Warburg syndrome or muscle-eye-brain disease, ISPD-related, muscular dystrophy-dystroglycanopathy, type A caused by mutation in ISPD.