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Charcot-Marie-Tooth disease axonal type 2CC

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Disease Overview

Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NEFH gene.

Synonyms

  • CMT2CC
  • Charcot-Marie-Tooth disease axonal type 2CC
  • Charcot-Marie-Tooth disease caused by mutation in NEFH
  • Charcot-Marie-Tooth disease, axonal, type 2CC
  • Charcot-Marie-Tooth disease, axonal, type 2cc
  • Charcot-Marie-Tooth neuropathy type 2CC
  • Charcot-Marie-Tooth neuropathy, type 2Cc
  • NEFH Charcot-Marie-Tooth disease
OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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