cushing disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Cushing disease (CD) is the most common cause of endogenous Cushing syndrome (CS; see this term) and is due to pituitary chronic over-secretion of ACTH by a pituitary corticotroph adenoma. (Orphanet Rare Disease Ontology, Orphanet_96253)
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Genes

1 genes associated with the disease cushing disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
GHR growth hormone receptor