| Metadata | |
|---|---|
| ID | DOID:0111206 |
| Name | autosomal dominant distal hereditary motor neuronopathy 2 |
| Definition | An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life. https://www.ncbi.nlm.nih.gov/pubmed/15122253, https://www.ncbi.nlm.nih.gov/pubmed/1517763 |
| Xrefs | |
| Alternateids |
DOID:0111208 |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal dominant adult spinal muscular atrophy IIA [EXACT] distal hereditary motor neuronopathy type 2 [EXACT] distal hereditary motor neuronopathy type 2A [EXACT] distal hereditary motor neuropathy type II [EXACT] distal hereditary motor neuropathy type IIA [EXACT] HMN II [EXACT] HMN IIA [EXACT] HMN2 [EXACT] HMN2A [EXACT] spinal Charcot-Marie-Tooth disease IIA [EXACT] |
| Parent Relationships |
is_a autosomal dominant distal hereditary motor neuronopathy |