Orphanet: Autosomal dominant Charcot Marie Tooth disease type 2K

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Autosomal dominant Charcot-Marie-Tooth disease type 2K

Disease definition

An axonal Charcot-Marie-Tooth (CMT) peripheral sensorimotor polyneuropathy.


Classification level: Disorder
  • Synonym(s):
    • CMT2K
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Childhood, Adolescent, Adult
  • ICD-10: G60.0
  • OMIM: 607831
  • UMLS: C1842983  C1842984
  • MeSH: -
  • GARD: 9199
  • MedDRA: -

Detailed information

Article for general public


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