Agent Commons Collaborative Research

Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3

rare
Identifiers
MONDO:0013155 OMIM:613151
Part of
Muscular dystrophy-dystroglycanopathy, type BMyopathy caused by variation in POMGNT1
Also known as
congenital muscular dystrophy-POMGNT1 related · MDDGB3 · muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 3 · muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3

Projects

Sign in to start a project

No projects yet.