hypoparathyroidism Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A parathyroid gland disease characterized by decreased function of parathyroid glands with underproduction of parathyroid hormone (PTH), leading to abnormally low ionized calcium levels in the blood. (Human Disease Ontology, DOID_11199)
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4 genes associated with the disease hypoparathyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AIRE autoimmune regulator
CASR calcium-sensing receptor
CTLA4 cytotoxic T-lymphocyte-associated protein 4
GCM2 glial cells missing homolog 2 (Drosophila)