Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 207
Gene Symbol: AKT1
AKT1
0.100 Biomarker disease HPO
Entrez Id: 210
Gene Symbol: ALAD
ALAD
0.210 AlteredExpression disease LHGDN Delta-aminolevulinate dehydratase (delta-ALA-D) activity in diabetes and hypothyroidism. 17291479 2007
Entrez Id: 210
Gene Symbol: ALAD
ALAD
0.210 Biomarker disease RGD Experimental hypothyroidism inhibits delta-aminolevulinate dehydratase activity in neonatal rat blood and liver. 17720948 2007
Entrez Id: 213
Gene Symbol: ALB
ALB
0.040 Biomarker disease BEFREE Hypothyroidism causes pericardial effusion through increased permeability of the epicardial vessels and decreased lymphatic drainage of albumin, resulting in accumulation of fluid in the pericardial space. 30948517 2019
Entrez Id: 213
Gene Symbol: ALB
ALB
0.040 AlteredExpression disease BEFREE A meta-analysis of the association of serum ischaemia-modified albumin levels with human hypothyroidism and hyperthyroidism. 27920278 2017
Entrez Id: 213
Gene Symbol: ALB
ALB
0.040 AlteredExpression disease BEFREE Multivariate logistic regression with adjustment for age, sex, kidney function, and serum albumin level showed that the odds ratios for overt hypothyroidism increased with increasing severity of hyponatremia when compared with Na ≥ 136 mEq/L (130-135 mEq/L: 1.43, 95% confidence interval [CI], 1.15 to 1.78, P = 0.001; ≤129 mEq/L: 1.87, 95% CI, 1.32 to 2.63, P < 0.001; P< 0.001 for trend). 30308047 2018
Entrez Id: 213
Gene Symbol: ALB
ALB
0.040 Biomarker disease BEFREE Higher proteinuria in patients with renal involvement and lower albumin in patients with hepatic involvement were associated with hypothyroidism. 28439924 2017
Entrez Id: 79053
Gene Symbol: ALG8
ALG8
0.100 Biomarker disease HPO
Entrez Id: 79053
Gene Symbol: ALG8
ALG8
0.100 CausalMutation disease CLINVAR
Entrez Id: 7840
Gene Symbol: ALMS1
ALMS1
0.100 Biomarker disease HPO
Entrez Id: 60529
Gene Symbol: ALX4
ALX4
0.100 Biomarker disease HPO
Entrez Id: 81693
Gene Symbol: AMN
AMN
0.010 Biomarker disease BEFREE This patient expands the phenotype X-AMN by adding growth hormone deficiency and hypothyroidism. 24685009 2014
Entrez Id: 27329
Gene Symbol: ANGPTL3
ANGPTL3
0.010 AlteredExpression disease BEFREE Serum Angptl3 and 8 levels were significantly higher in the hypothyroid groups compared to the control group (<i>p</i> < 0.05). 31380419 2019
Entrez Id: 55908
Gene Symbol: ANGPTL8
ANGPTL8
0.010 Biomarker disease BEFREE Circulating Angptl3 and Angptl8 Are Increased in Patients with Hypothyroidism. 31380419 2019
Entrez Id: 118429
Gene Symbol: ANTXR2
ANTXR2
0.010 AlteredExpression disease BEFREE Hypertension, hypothyroidism and HFS were observed most frequently, in about two-thirds of the patients. 30666498 2019
Entrez Id: 301
Gene Symbol: ANXA1
ANXA1
0.200 Biomarker disease RGD In vivo modulation of annexins I, II and V expression by thyroxine and methylthiouracil. 9022675 1996
Entrez Id: 302
Gene Symbol: ANXA2
ANXA2
0.200 Biomarker disease RGD In vivo modulation of annexins I, II and V expression by thyroxine and methylthiouracil. 9022675 1996
Entrez Id: 308
Gene Symbol: ANXA5
ANXA5
0.200 Biomarker disease RGD In vivo modulation of annexins I, II and V expression by thyroxine and methylthiouracil. 9022675 1996
Entrez Id: 324
Gene Symbol: APC
APC
0.100 Biomarker disease HPO
Entrez Id: 335
Gene Symbol: APOA1
APOA1
0.010 GeneticVariation disease BEFREE In the present study, we studied whether plasma levels of high-density lipoprotein-cholesterol (HDL-C) and apolipoprotein A-I (Apo A-I) were altered in patients with HO, and if so, whether this change was mediated by HHcy. 27457726 2016
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
0.200 Biomarker disease RGD Thyroid hormone regulates the hypotriglyceridemic gene APOA5. 15941710 2005
Entrez Id: 338
Gene Symbol: APOB
APOB
0.010 GeneticVariation disease BEFREE To assess whether the variable extent to which patients with hypothyroidism become hypercholesterolemic was associated with variation in the genes for the low density lipoprotein (LDL) receptor or apolipoprotein-B, we investigated prospectively 52 patients with primary hypothyroidism treated with L-T4. 8100826 1993
Entrez Id: 55911
Gene Symbol: APOBR
APOBR
0.010 Biomarker disease BEFREE Two variants, the fatty acid synthase (FASN) and apolipoprotein B receptor (APOBR) genes, were further analyzed, as they were highly associated with hypothyroidism. 30272292 2018
Entrez Id: 345
Gene Symbol: APOC3
APOC3
0.200 Biomarker disease RGD We therefore measured the transcriptional activity of the apoA-IV and apoC-III genes and the abundance of their nuclear RNA and total cellular mRNA in livers of control rats and rats made hyper- and hypothyroid. 8429259 1993
Entrez Id: 348
Gene Symbol: APOE
APOE
0.310 GeneticVariation disease BEFREE In females, there was an ApoE allele effect on thyroid status (P < or = 0.01), E2 being negatively (P < or = 0.01) and E4 being positively (P < or = 0.05) associated with "hypothyroidism". 12833399 2003