increased circulating acth level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal increased in the concentration of corticotropin, also known as adrenocorticotropic hormone (ACTH), in the blood. (Human Phenotype Ontology, HP_0003154)
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4 genes associated with the increased circulating acth level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MRAP melanocortin 2 receptor accessory protein
POR P450 (cytochrome) oxidoreductase