Type 6 Charcot-Marie-Tooth Disease

About the Disease
Neuropathy, Hereditary Motor and Sensory, Type Via, with Optic Atrophy, also known as peripheral neuropathy and optic atrophy, is related to charcot-marie-tooth disease type 2a2a and motor peripheral neuropathy. An important gene associated with Neuropathy, Hereditary Motor and Sensory, Type Via, with Optic Atrophy is MFN2 (Mitofusin 2), and among its related pathways/superpathways is Mitochondrial translation. Affiliated tissues include brain and peripheral nerve, and related phenotypes are mild neurosensory hearing impairment and scoliosis

Common Targets
PDK3 | MTRFR

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