Congenital Hypoparathyroidism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Deficiency of parathyroid hormone with congenital onset. (Human Phenotype Ontology, HP_0008198)
External Link https://www.disgenet.org/browser/0/1/0/C1455734
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Genes

5 genes associated with the disease Congenital Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
FAM111A family with sequence similarity 111, member A
GCM2 glial cells missing homolog 2 (Drosophila)
GH1 growth hormone 1
PTH parathyroid hormone
TBCE tubulin folding cofactor E