Neuronopathy, distal hereditary motor, autosomal dominant 1

MONDO:0008451

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

Also known as: Charcot-Marie-Tooth disease, spinal, I, DHMN1, autosomal dominant distal juvenile spinal muscular atrophy type 1, dHMN1, distal hereditary motor neuronopathy type I, neuronopathy, distal hereditary motor, type 1, Charcot-Marie-Tooth disease, spinal, 1, HMN 1

18 clinical trials for this condition and its sub-types, 0 tagged with Neuronopathy, distal hereditary motor, autosomal dominant 1 itself.

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↑ Charcot-Marie-Tooth disease (78) ↑ Neuronopathy, distal hereditary motor, autosomal dominant (0)

Including sub-types (18) Tagged with Neuronopathy, distal hereditary motor, autosomal dominant 1 (0)

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