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Charcot-Marie-Tooth disease, type 1

Orpha number ORPHA65753
Prevalence of rare diseases 1-5 / 10 000
Inheritance
  • Autosomal dominant
Age of onset Variable
ICD 10 code
  • G60.0
MIM number -
Synonym(s) CMT1
Charcot-Marie-Tooth disease, demyelinating, autosomal dominant
Hereditary motor and sensory neuropathy, type 1

Summary


An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.




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.
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