Variants
Sign InSign Up

Charcot-Marie-Tooth disease axonal type 2CC

Your Results

Sign In

Description

Axonal Charcot-Marie-Tooth disease type 2CC is an autosomal dominant peripheral neuropathy that predominantly affects the lower limbs, resulting in muscle weakness and atrophy and gait impairment. Other features include distal sensory impairment and less severe involvement of the upper limbs. The age at onset and severity are variable (summary by Rebelo et al., 2016). For a phenotypic description and a discussion of genetic heterogeneity of axonal CMT type 2, see CMT2A (118210).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

7

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    616924

  • Orphanet
  • HPO
  • Medgen

    C4310790

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.