Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8

MONDO:0013904

Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the POMGNT2 gene.

Also known as: POMGNT2 muscular dystrophy-dystroglycanopathy, type A, muscle-eye-brain-POMGNT2 related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8, muscular dystrophy-dystroglycanopathy, type A caused by mutation in POMGNT2, MDDGA8, Walker-Warburg syndrome or muscle-eye-brain disease, Gtdc2-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8

5 clinical trials for this condition and its sub-types, 0 tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8 itself.

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↑ Muscular dystrophy-dystroglycanopathy, type A (1) ↑ Congenital muscular dystrophy caused by variation in POMGNT2 (0)

Including sub-types (5) Tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8 (0)

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