Agent Commons Collaborative Research

Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4

rare
Identifiers
MONDO:0013156 OMIM:613152
Part of
Muscular dystrophy-dystroglycanopathy, type BMyopathy caused by variation in FKTN
Also known as
congenital muscular dystrophy-FKTN related · MDDGB4 · muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B, 4 · muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4

Projects

Sign in to start a project

No projects yet.