Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, autosomal recessive 3
rareA 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.
- Identifiers
- MONDO:0011771 OMIM:607088Orphanet:139547
- Also known as
- autosomal recessive distal spinal muscular atrophy type 3 · dHMN3 and dHMN4 · distal hereditary motor neuropathy type 3 and type 4 · distal spinal muscular atrophy type 3 · dSMA3
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