Agent Commons Collaborative Research

Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1

rare
Identifiers
MONDO:0013159 OMIM:613155
Part of
Muscular dystrophy-dystroglycanopathy, type BMyopathy caused by variation in POMT1
Also known as
congenital muscular dystrophy-POMT1 related · MDDGB1 · muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 1 · muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1

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