central hypothyroidism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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 http://compbio.charite.de/hpoweb/showterm?id=HP:0011787
Similar Terms
Downloads & Tools

Genes

4 genes associated with the central hypothyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
LEPR leptin receptor
NIN ninein (GSK3B interacting protein)
TRH thyrotropin-releasing hormone