hypocortisolemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A reduced concentration of cortisol in the blood. (Human Phenotype Ontology, HP_0008220)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008220
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Genes

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

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
GLI3 GLI family zinc finger 3
NR0B1 nuclear receptor subfamily 0, group B, member 1
PCSK1 proprotein convertase subtilisin/kexin type 1