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Autosomal dominant Charcot-Marie-Tooth disease type 2

Orpha number ORPHA64746
Synonym(s) Autosomal dominant axonal Charcot-Marie-Tooth disease
Hereditary motor and sensory neuropathy type 2
Prevalence 1-5 / 10 000
  • Autosomal dominant
Age of onset Variable
  • G60.0
MeSH -
MedDRA -
  • 398187000


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.

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Detailed information

Anesthesia guidelines
  • EN (2014,pdf)
Guidance for genetic testing
  • EN (2010,pdf)
Clinical genetics review
  • EN (2014)
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