Congenital Hypothyroidism Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A hypothyroidism that is present at birth. (Human Disease Ontology, DOID_0050328)
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Genes

12 genes associated with the Congenital Hypothyroidism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
DUOX2 dual oxidase 2
DUOXA2 dual oxidase maturation factor 2
FOXE1 forkhead box E1
NKX2-1 NK2 homeobox 1
NKX2-5 NK2 homeobox 5
PAX8 paired box 8
TG thyroglobulin
TPO thyroid peroxidase
TSHB thyroid stimulating hormone, beta
TSHR thyroid stimulating hormone receptor
TTF1 transcription termination factor, RNA polymerase I
TTF2 transcription termination factor, RNA polymerase II