Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 09-03-2009

Symbol	HMSN6
Location	1p36.22
Name	hereditary motor and sensory neuropathy VI
Other name(s)	peripheral neuropathy and optic atrophy Charcot-Marie-Tooth disease, type 6
Corresponding gene	MFN2
Other symbol(s)	HMSN VI, CMT6
Genetic determination	autosomal dominant
Related entries	allelis disorder: CMT2A2
Function/system disorder	neurology
	eye
Type	disease

Remark(s)

HMSN VI might be a variant of the early onset severe CMT2A phenotype.