paroxysmal dyskinesia Gene Set

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
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Genes

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