|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A reduced ability to secrete adrenocorticotropic hormone (ACTH), a hormone that stimulates the adrenal cortex to secrete of glucocorticoids such as cortisol. (Human Phenotype Ontology, HP_0011748)|
|Downloads & Tools|
2 genes associated with the adrenocorticotropic hormone deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.