Congenital Central Hypothyroidism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4302200
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Genes

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

Symbol Name
BRD2 bromodomain containing 2
IGSF1 immunoglobulin superfamily, member 1
IRS4 insulin receptor substrate 4
PRL prolactin
SERPINA7 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7
TRH thyrotropin-releasing hormone
TRHR thyrotropin-releasing hormone receptor
TSHB thyroid stimulating hormone, beta