Adrenal Insufficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Insufficient production of steroid hormones (primarily cortisol) by the adrenal glands as a result of a primary defect in the glands themselves. (Human Phenotype Ontology, HP_0000846)
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Genes

7 genes associated with the Adrenal Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
CIITA class II, major histocompatibility complex, transactivator
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
NR5A1 nuclear receptor subfamily 5, group A, member 1
PIN1 peptidylprolyl cis/trans isomerase, NIMA-interacting 1