Skip to
  1. Homepage
  2. Rare diseases
  3. Search
PrintPrint
Simple search

Simple search

*
(*) mandatory field





Other search option(s)

Charcot-Marie-Tooth disease

Orpha number ORPHA166
Prevalence of rare diseases 1-5 / 10 000
Inheritance
  • X-linked dominant
  • Autosomal dominant
  • X-linked recessive
  • Autosomal recessive
Age of onset Variable
ICD 10 code
  • G60.0
MIM number -
Synonym(s) CMT
Charcot-Marie-Tooth hereditary neuropathy

Summary

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, search for in the “Classifications” menu.

Detailed information

Review article
Get Acrobat Reader
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Languages :