Central Hypothyroidism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of hypothyroidism due to an insufficient stimulation of an otherwise normal thyroid gland. Central hypothyroidism is caused by either pituitary (secondary hypothyroidism) or hypothalamic (tertiary hypothyroidism) defects. (Human Phenotype Ontology, HP_0011787)
External Link https://www.disgenet.org/browser/0/1/0/C0271801
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Genes

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

Symbol Name
ACE angiotensin I converting enzyme
ARID1A AT rich interactive domain 1A (SWI-like)
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
DMXL2 Dmx-like 2
ELN elastin
GH1 growth hormone 1
GHRHR growth hormone releasing hormone receptor
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HESX1 HESX homeobox 1
IGSF1 immunoglobulin superfamily, member 1
KIAA0556 KIAA0556
LEPR leptin receptor
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
MAGEL2 melanoma antigen family L2
NCOR2 nuclear receptor corepressor 2
NIN ninein (GSK3B interacting protein)
POMC proopiomelanocortin
POU1F1 POU class 1 homeobox 1
PRL prolactin
PROP1 PROP paired-like homeobox 1
RALGAPB Ral GTPase activating protein, beta subunit (non-catalytic)
SETBP1 SET binding protein 1
SLC20A1 solute carrier family 20 (phosphate transporter), member 1
SLC30A10 solute carrier family 30, member 10
SOD1 superoxide dismutase 1, soluble
SST somatostatin
TBL1X transducin (beta)-like 1X-linked
TNF tumor necrosis factor
TRH thyrotropin-releasing hormone
TRHR thyrotropin-releasing hormone receptor
TSHB thyroid stimulating hormone, beta
XPR1 xenotropic and polytropic retrovirus receptor 1