adrenocorticotropic hormone deficiency Gene Set

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
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Genes

1 genes associated with the adrenocorticotropic hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TBX19 T-box 19