distal hereditary motor neuronopathy type 7 (Q66084895)
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autosomal dominant distal hereditary motor neuronopathy characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis
- dHMN7
- distal spinal muscular atrophy with vocal cord paralysis
- DHMNVPy
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | distal hereditary motor neuronopathy type 7 |
autosomal dominant distal hereditary motor neuronopathy characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis |
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