primary hypercorticolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hypercortisolemia associated with a primary defect of the adrenal gland leading to overproduction of cortisol. (Human Phenotype Ontology, HP_0001579)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001579
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Genes

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

Symbol Name
GNAS GNAS complex locus
PDE11A phosphodiesterase 11A
PRKACA protein kinase, cAMP-dependent, catalytic, alpha
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha