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Charcot-Marie-Tooth disease type 4

Disease definition

A disorder that belongs to the genetically heterogeneous group of CMT peripheral sensorimotor polyneuropathy diseases.

ORPHA:64749

Classification level: Group of disorders
  • Synonym(s):
    • AR-CMT1
    • Autosomal recessive demyelinating Charcot-Marie-Tooth
    • CMT4
  • Prevalence: 1-5 / 10 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Childhood
  • ICD-10: G60.0
  • OMIM: -
  • UMLS: -
  • MeSH: -
  • GARD: 12440
  • MedDRA: -

Detailed information

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