| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Episodic bouts of involuntary movements with dystonic, choreic, ballistic movements, or a combination thereof. There is no loss of consciousness during the attacks. (Human Phenotype Ontology, HP_0007166) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0007166 |
| Similar Terms | |
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1 genes associated with the paroxysmal dyskinesia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| KCNMA1 | potassium channel, calcium activated large conductance subfamily M alpha, member 1 |
