distal hereditary motor neuronopathy type 8 (Q66084911)
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human disease
- autosomal dominant benign distal spinal muscular atrophy
- HMN8
- DHMN8
- congenital benign spinal muscular atrophy with contractures
- distal hereditary motor neuropathy type VIII
- autosomal dominant congenital benign spinal muscular atrophy
- congenital nonprogressive spinal muscular atrophy
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | distal hereditary motor neuronopathy type 8 |
human disease |
|
Statements
1 reference
Identifiers
1 reference
1 reference