DO_rare_slim has material basis in has symptom disease has basis in Fukuyama congenital muscular dystrophy disease_ontology DOID:0050559 ORDO:272 MIM:253800 A congenital muscular dystrophy-dystroglycanopathy type A that is characterized by muscle weakness, failure to thrive, severe intellectual and developmental disability, impaired vision and cardiac abnormalities and has_material_basis_in mutation in the FKTN gene that produces the fukutin protein. GARD:6475 OMIM mapping confirmed by DO. [SN]. congenital muscular dystrophy-dystroglycanopathy type A autosomal recessive inheritance Abnormality of prenatal development or birth muscle weakness