Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Hereditary neuromuscular disease
/
Hereditary peripheral neuropathy
/
Charcot-Marie-Tooth disease
/
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease, axonal, type 2EE
rare
Identifiers
MONDO:0032728
OMIM:618400
Causal genes
MPV17
Part of
Charcot-Marie-Tooth disease type 2
Also known as
CMT2EE
Projects
Sign in to start a project
No projects yet.