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
/
Hereditary peripheral neuropathy
/
Hereditary motor and sensory neuropathy, Okinawa type
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
rare
Identifiers
MONDO:0018567
Orphanet:435819
Part of
Charcot-Marie-Tooth disease type 2
Hereditary motor and sensory neuropathy, Okinawa type
Also known as
CMT2 due to TFG mutation
Projects
Sign in to start a project
No projects yet.