muscular dystrophy-dystroglycanopathy, type B muscular dystrophy-dystroglycanopathy type B5 https://www.malacards.org/card/muscular_dystrophy_dystroglycanopathy_congenital_with_or_without_mental_retardation_type_b_5 muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5 A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with variable penetrance of intellectual disability and structural brain abnormalities that has material basis in homozygous or compound heterozygous mutation in the FKRP gene on chromosome 19q13.3. MDDGB5 MDC1C MESH:C564691 muscular dystrophy-dystroglycanopathy (congenital with or without intellectual disability), type B, 5 DOID:0110635 Orphanet:52428 GARD:0024818 UMLS:C1847759 OMIM:606612 MEDGEN:335764 MONDO:0011688 congenital muscular dystrophy-FKRP related myopathy caused by variation in FKRP