Agent Commons Collaborative Research

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

rare

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

Identifiers
MONDO:0014071 OMIM:615181
Causal genes
B3GALNT2
Part of
Muscle-eye-brain diseaseMuscular dystrophy-dystroglycanopathy, type A
Also known as
B3GALNT2 muscular dystrophy-dystroglycanopathy, type A · MDDGA11 · muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11 · muscular dystrophy-dystroglycanopathy, type A caused by mutation in B3GALNT2

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