Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10

MONDO:0014022

Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the RXYLT1 gene.

Also known as: RXYLT1 muscular dystrophy-dystroglycanopathy, type A, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10, muscular dystrophy-dystroglycanopathy, type A caused by mutation in RXYLT1, MDDGA10, Walker-Warburg syndrome or muscle-eye-brain disease, Tmem5-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10

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