| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A type of dysarthria related to bilateral damage of the upper motor neuron tracts of the pyramidal and extra- pyramidal tracts. Speech of affected individuals is slow, effortful, and has a harsh vocal quality. (Human Phenotype Ontology, HP_0002464) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0002464 |
| Similar Terms | |
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1 genes associated with the spastic dysarthria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ALS2 | amyotrophic lateral sclerosis 2 (juvenile) |