Search
Charcot-Marie-Tooth disease type 6; autosomal dominant hereditary motor & sensory neuropathy VI (CMT6, HMSN6)
Also see Charcot-Marie-Tooth disease
Pathology:
- axonal form of Charcot-Marie-Tooth disease associated with optic atrophy
Genetics:
1) autosomal dominant
2) associated with defects in MFN2
Database Correlations
OMIM 601152
References
OMIM :accession 601152