abnormality of circulating cortisol level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the concentration of cortisol in the blood. (Human Phenotype Ontology, HP_0011731)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011731
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6 genes associated with the abnormality of circulating cortisol level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GNAS GNAS complex locus
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MRAP melanocortin 2 receptor accessory protein
PDE11A phosphodiesterase 11A
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
TBX19 T-box 19