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

MONDO:0014071

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

Also known as: B3GALNT2 muscular dystrophy-dystroglycanopathy, type A, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11, muscular dystrophy-dystroglycanopathy, type A caused by mutation in B3GALNT2, MDDGA11, Walker-Warburg syndrome or muscle-eye-brain disease, B3Galnt2-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 11

39 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by