Fukuyama type muscular dystrophy (FCMD) is a congenital progressive muscular dystrophy characterized by brain malformation (cobblestone lissencephaly), dystrophic changes in skeletal muscle, severe intellectual deficit, epilepsy and motor impairment. The disease is muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 (MONDO_0009678, a Monarch Disease Ontology term). Also known as: FCMD, Fukuyama Type Congenital Muscular Dystrophy, Fukuyama congenital muscular dystrophy, MDDGA4, Walker-Warburg syndrome or muscle-eye-brain disease, FKTN-related, muscle-eye-brain-FKTN related, muscular dystrophy-dystroglycanopathy (congenital with Brain and eye anomalies) type A, 4.