hypoparathyroidism Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
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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Genes

9 genes co-occuring with the biological term hypoparathyroidism in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
AP2S1	adaptor-related protein complex 2, sigma 1 subunit
CASR	calcium-sensing receptor
FGF23	fibroblast growth factor 23
GATA3	GATA binding protein 3
GCM2	glial cells missing homolog 2 (Drosophila)
GNA11	guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
NLRP5	NLR family, pyrin domain containing 5
PTH	parathyroid hormone
PTPN22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)