paroxysmal choreoathetosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Episodes of choreoathetosis that can occur following triggers such as quick voluntary movements. (Human Phenotype Ontology, HP_0007098)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007098
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Genes

2 genes associated with the paroxysmal choreoathetosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PNKD paroxysmal nonkinesigenic dyskinesia
PRRT2 proline-rich transmembrane protein 2