periodic hypokalemic paresis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Episodes of muscle weakness associated with reduced levels of potassium in the blood. (Human Phenotype Ontology, HP_0008153)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008153
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Genes

3 genes associated with the periodic hypokalemic paresis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CA2 carbonic anhydrase II
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)