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Up to: Muscular dystrophy-dystroglycanopathy, type A · Myopathy caused by variation in CRPPA
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the ISPD gene.
This condition has no sub-types.