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Up to: Myopathy caused by variation in FKRP · Muscular dystrophy-dystroglycanopathy, type B
Muscular dystrophy-dystroglycanopathy type B5
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.
This condition has no sub-types.