neuronopathy, distal hereditary motor, autosomal recessive 3
MONDO:0011771Mondo
Findings
No curated finding names neuronopathy, distal hereditary motor, autosomal recessive 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A rare neuromuscular disease characterized by progressive muscular weakness and atrophy predominantly affecting distal parts of limbs, later involvement of proximal and trunk muscles with marked hyperlordosis and late diaphragmatic dysfunction.
Definition from the Mondo Disease Ontology (MONDO:0011771), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
6 names
Resolves to: neuronopathy, distal hereditary motor, autosomal recessive 3
- Also called
- autosomal recessive distal spinal muscular atrophy type 3dHMN3 and dHMN4distal hereditary motor neuropathy type 3 and type 4distal spinal muscular atrophy type 3dSMA3spinal muscular atrophy, chronic distal, autosomal recessive