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Up to: Muscular dystrophy-dystroglycanopathy, type A · Muscle-eye-brain disease
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the RXYLT1 gene.
This condition has no sub-types.