Variants
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Charcot-Marie-Tooth disease type 2J

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Description

For a phenotypic description and a discussion of genetic heterogeneity of axonal CMT, see CMT2A1 (118210).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

11

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    607736

  • Orphanet

    99943

  • HPO
  • Medgen

    C1843153

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