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Charcot-Marie-Tooth disease, type I

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Description

Charcot-Marie-Tooth disease type 1 (CMT1) is a group of autosomal dominant demyelinating peripheral neuropathies characterized by distal weakness and atrophy, sensory loss, foot deformities, and slow nerve conduction velocity.

ORDO

  • Mode of Inheritance

    VARIANTS

    456

    SEE THE VARIANTS →

    Genes

    External Links

    • OMIM
    • Orphanet

      65753

    • HPO
    • Medgen

      C0751036

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