|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the paroxysmal dyskinesia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|KCNMA1||potassium channel, calcium activated large conductance subfamily M alpha, member 1|