Charcot-Marie-Tooth disease type 1

MONDO:0019011

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.

Also known as: CMT1, Charcot-Marie-Tooth neuropathy type 1, autosomal dominant demyelinating Charcot-Marie-Tooth disease, hereditary motor and sensory neuropathy type 1, Charcot-Marie-Tooth type 1

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