Hypoparathyroidism Gene Set

Dataset CTD 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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007011
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Genes

1 genes/proteins associated with the disease Hypoparathyroidism from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CASR calcium-sensing receptor 2.88009