Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Muscular dystrophy-dystroglycanopathy, type A · Congenital muscular dystrophy caused by variation in POMGNT2
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the POMGNT2 gene.
This condition has no sub-types.