|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Adrenal insufficiency secondary to a defect in the ACTH receptor. (Human Phenotype Ontology, HP_0008259)|
|Downloads & Tools|
1 genes associated with the adrenocorticotropin (acth) receptor (acthr) defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|AAAS||achalasia, adrenocortical insufficiency, alacrimia|