Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12

MONDO:0014101

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

Also known as: POMK muscular dystrophy-dystroglycanopathy, type A, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12, muscular dystrophy-dystroglycanopathy, type A caused by mutation in POMK, MDDGA12, Walker-Warburg syndrome or muscle-eye-brain disease, POMK-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12

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