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GENATLAS PHENOTYPE
last update : 20/06/2006
Symbol CMT2I
Location 1q22
Name Charcot-Marie-Tooth disease, axonal, type 2I
Other name(s) Charcot-Marie-Tooth neuropathy, type 2I
Corresponding gene MPZ
Main clinical features
  • prominent sensory involvement, very late onset, progressive, leading to marked disability
    • Genetic determination
    Function/system disorder neurology
    Type disease
    Gene product
    Name myelin protein zero