Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Hereditary neuromuscular disease
/
Autosomal recessive limb-girdle muscular dystrophy
Muscular dystrophy, limb-girdle, autosomal recessive 26
rare
Identifiers
MONDO:0030014
OMIM:618848
Causal genes
POPDC3
Part of
Autosomal recessive limb-girdle muscular dystrophy
Also known as
LGMDR26
Projects
Sign in to start a project
No projects yet.