Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7

MONDO:0013835

Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the ISPD gene.

Also known as: ISPD muscular dystrophy-dystroglycanopathy, type A, Walker-Warburg syndrome or muscle-eye-brain disease, ISPD-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, muscular dystrophy-dystroglycanopathy, type A caused by mutation in ISPD, MDDGA7

5 clinical trials for this condition and its sub-types, 0 tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7 itself.

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↑ Muscular dystrophy-dystroglycanopathy, type A (1) ↑ Myopathy caused by variation in CRPPA (1)

Including sub-types (5) Tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7 (0)

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