Hyperparathyroidism Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A parathyroid gland disease characterized by an overactivity of the parathyroid glands, leading to an excess of parathyroid hormone in the body. (Human Disease Ontology, DOID_13543)
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11 genes associated with the Hyperparathyroidism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CASR calcium-sensing receptor
CCND1 cyclin D1
CDC73 cell division cycle 73
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CSNK1D casein kinase 1, delta
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
FRA1H fragile site, 5-azacytidine type, common, fra(1)(q42)
LEPR leptin receptor
MEN1 multiple endocrine neoplasia I
RET ret proto-oncogene
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor