Charcot-Marie-Tooth disease type 2

MONDO:0018993

A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.

Also known as: CMT2, autosomal dominant axonal Charcot-Marie-Tooth disease, hereditary motor and sensory neuropathy type 2, Charcot-Marie-Tooth type 2, autosomal dominant Charcot-Marie-Tooth disease type 2

16 clinical trials for this condition and its sub-types.

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