Charcot-Marie-Tooth Disease Type 4D

About the Disease
Charcot-Marie-Tooth Disease, Type 4d, also known as charcot-marie-tooth disease type 4d, is related to hereditary sensory neuropathy and hereditary neuropathies. An important gene associated with Charcot-Marie-Tooth Disease, Type 4d is NDRG1 (N-Myc Downstream Regulated 1), and among its related pathways/superpathways are Glycerophospholipid biosynthesis and PI Metabolism. Affiliated tissues include tongue, bone and peripheral nerve, and related phenotypes are decreased motor nerve conduction velocity and distal lower limb muscle weakness

Common Targets
NDRG1 | REEP1

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