Charcot-Marie-Tooth disease type 6; autosomal dominant hereditary motor & sensory neuropathy VI (CMT6, HMSN6)

Introduction

Also see Charcot-Marie-Tooth disease

Pathology

• axonal form of Charcot-Marie-Tooth disease associated with optic atrophy

Genetics

• autosomal dominant
• associated with defects in MFN2

More general terms

• Charcot-Marie-Tooth disease

Database

• OMIM: https://mirror.omim.org/entry/601152