hypoaldosteronism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally reduced levels of aldosterone. (Human Phenotype Ontology, HP_0004319)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004319
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Genes

7 genes associated with the hypoaldosteronism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
AIRE autoimmune regulator
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
NR0B1 nuclear receptor subfamily 0, group B, member 1
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit