adrenocorticotropin (acth) receptor (acthr) defect Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Adrenal insufficiency secondary to a defect in the ACTH receptor. (Human Phenotype Ontology, HP_0008259)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008259
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Genes

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.

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia