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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
    Type disease
    Remark(s) HMSN VI might be a variant of the early onset severe CMT2A phenotype.