muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11

Rare Disease

MONDO:0014071

Also known as:

B3GALNT2 muscular dystrophy-dystroglycanopathy, type Amuscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11

Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the B3GALNT2 gene.

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