| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://www.omim.org/entry/201400 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the adrenocorticotropic hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TBX19 | T-box 19 |
