WormBase Tree Display for DO_term: DOID:0111199
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| DOID:0111199 | Name | distal hereditary motor neuronopathy type 7 | |
|---|---|---|---|
| Status | Valid | ||
| Definition | An 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. | ||
| Synonym | Exact | DHMNVPy | |
| dHMN7 | |||
| distal spinal muscular atrophy with vocal cord paralysis | |||
| Parent | Is_a | DOID:0111198 | |
| Child | Is | DOID:0111202 | |
| DOID:0111201 |
