neuronopathy, distal hereditary motor, autosomal dominant 1
MONDO:0008451Mondo
Findings
No curated finding names neuronopathy, distal hereditary motor, autosomal dominant 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration.
Definition from the Mondo Disease Ontology (MONDO:0008451), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
5 names
Resolves to: neuronopathy, distal hereditary motor, autosomal dominant 1
- Also called
- autosomal dominant distal juvenile spinal muscular atrophy type 1Charcot-Marie-Tooth disease, spinal, IDHMN1distal hereditary motor neuronopathy type Ineuronopathy, distal hereditary motor, type 1