|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Abnormally increased concentration of cortisol in the urine. (Human Phenotype Ontology, HP_0012030)|
|Downloads & Tools|
1 genes associated with the increased urinary cortisol level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|NR3C1||nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)|