Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
0.100 Biomarker disease HPO
Entrez Id: 2688
Gene Symbol: GH1
GH1
0.010 GeneticVariation disease BEFREE Twenty-one of 48 (44%) participants had a subnormal response to GH stimulation; 19 of 53 (36%) had overt or compensated hypothyroidism, while 8 of 40 participants had reduced thyroid-hormone binding. 11335753 2001
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10
0.100 Biomarker disease HPO
Entrez Id: 7080
Gene Symbol: NKX2-1
NKX2-1
0.100 Biomarker disease HPO
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
0.100 Biomarker disease HPO
Entrez Id: 7038
Gene Symbol: TG
TG
0.110 GeneticVariation disease BEFREE Biallelic mutations in the Tg gene have been identified in several animal species and human patients presenting with goiter and overt or compensated hypothyroidism. 16187910 2005
Entrez Id: 7038
Gene Symbol: TG
TG
0.110 Biomarker disease HPO
Entrez Id: 7253
Gene Symbol: TSHR
TSHR
0.020 GeneticVariation disease BEFREE Our observations also suggest that heterozygosity for an inactivating TSHR mutation may be associated with compensated hypothyroidism and thyroid hypoplasia. 14725684 2004
Entrez Id: 7253
Gene Symbol: TSHR
TSHR
0.020 GeneticVariation disease BEFREE Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese. 17526952 2006