|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Hypercortisolemia associated with a primary defect of the adrenal gland leading to overproduction of cortisol. (Human Phenotype Ontology, HP_0001579)|
|Downloads & Tools|
4 genes associated with the primary hypercorticolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.