episodic quadriplegia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Intermittent episodes of paralysis of all four limbs. (Human Phenotype Ontology, HP_0200072)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0200072
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Genes

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

Symbol Name
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide