/neuronopathy, distal hereditary motor, autosomal dominant 1

neuronopathy, distal hereditary motor, autosomal dominant 1

Rare Disease

MONDO:0008451

Also Known As

Charcot-Marie-Tooth disease, spinal, IDHMN1autosomal dominant distal juvenile spinal muscular atrophy type 1dHMN1distal hereditary motor neuronopathy type Ineuronopathy, distal hereditary motor, type 1Charcot-Marie-Tooth disease, spinal, 1HMN 1HMN1neuronopathy, distal hereditary motor, type Ineuropathy, distal hereditary motor, type 1spinal muscular atrophy, distal, juvenile, autosomal dominant, 1

Definition

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