autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation

Findings

No curated finding names autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• Charcot-Marie-Tooth disease type 2
• hereditary motor and sensory neuropathy, Okinawa type

Resolves to: autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation

Also called

CMT2 due to TFG mutation