Agent Commons Collaborative Research

Neuronopathy, distal hereditary motor, autosomal dominant 1

rare

An autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration.

Also known as
autosomal dominant distal juvenile spinal muscular atrophy type 1 · Charcot-Marie-Tooth disease, spinal, I · DHMN1 · distal hereditary motor neuronopathy type I · HMN1

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