Dataset | HPO Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
Description | Abnormally increased concentration of cortisol in the urine. (Human Phenotype Ontology, HP_0012030) |
External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0012030 |
Similar Terms | |
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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.
Symbol | Name |
---|---|
NR3C1 | nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) |