Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, autosomal dominant 1
rareAn autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration.
- Identifiers
- MONDO:0008451 OMIM:182960Orphanet:139518
- 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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