muscular dystrophy-dystroglycanopathy, type A muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/muscular_dystrophy_dystroglycanopathy_congenital_with_brain_and_eye_anomalies_type_a_4 MEDGEN:140820 muscular dystrophy-dystroglycanopathy (congenital with Brain and eye anomalies) type A, 4 DOID:0050559 Fukuyama congenital muscular dystrophy muscle-eye-brain-FKTN related GARD:0006475 OMIM:253800 Orphanet:272 MONDO:0009678 Fukuyama Type Congenital Muscular Dystrophy muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 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. MDDGA4 SCTID:111502003 NCIT:C126741 FCMD UMLS:C0410174 NANDO:2200860 Walker-Warburg syndrome or muscle-eye-brain disease, FKTN-related NANDO:1200494 NORD:1169 muscle-eye-brain disease myopathy caused by variation in FKTN