Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Endothelial nitric oxide synthase genetic variation and essential hypertension risk in Han Chinese: the Fangshan study. 18769442

2009

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Endothelial nitric oxide synthase gene haplotypes and circulating nitric oxide levels significantly associate with risk of essential hypertension. 18325347

2008

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN The 894T and -786C alleles of the NOS3 gene were significantly associated with both hypertension and CVD in renal allograft recipients. 18331440

2008

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN In summary, the NOS3 IVS25+15 is directly associated with blood pressure and hypertension in white Europeans. 18246059

2008

Entrez Id: 3291
Gene Symbol: HSD11B2
HSD11B2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 PosttranslationalModification LHGDN These results show a clear link between the epigenetic regulation through repression of HSD11B2 in PBMC DNA and hypertension. 18178212

2008

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Association of eNOS Glu298Asp gene polymorphism with essential hypertension in Asian Indians. 17935708

2008

Entrez Id: 2908
Gene Symbol: NR3C1
NR3C1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN A novel point mutation in the amino terminal domain of the human glucocorticoid receptor (hGR) gene enhancing hGR-mediated gene expression. 18827003

2008

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 AlteredExpression LHGDN The current exploratory work describes that the activity of MMP-2 in the internal mammary artery is correlated with age, hypertension, diabetes and eGFR. 18332634

2008

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 Biomarker LHGDN Activation of proMMP-2 and Src by HHV8 vGPCR in human pulmonary arterial endothelial cells. 17188706

2007

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Lack of association between endothelial nitric oxide synthase gene polymorphisms, microalbuminuria and endothelial dysfunction in hypertensive men. 17563560

2007

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN NOS3 T-786C was also related to hypertension (p=0.049). 17126309

2007

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN It was found that the frequencies of b/b, b/a and a/a genotypes of the eNOS4 gene were 84.06%, 15.22% and 0.72% in the control group, and 81.46%, 15.89% and 2.65% in the hypertension group, respectively. 17492127

2007

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Association of endothelial nitric oxide synthase gene G894T polymorphism with essential hypertension in an adult Pakistani Pathan population. 16765468

2007

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN While endothelial nitric oxide synthase (eNOS) haplotypes have been associated with HT, it is unknown whether eNOS genotypes/haplotypes are associated with altered susceptibility to HT in patients with T2DM. 16427644

2006

Entrez Id: 3291
Gene Symbol: HSD11B2
HSD11B2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN In AME, defective HSD11B2 enzyme activity results in overstimulation of the mineralocorticoid receptor (MR) by cortisol, causing sodium retention, hypokalemia, and salt-dependent hypertension. 16778331

2006

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 Biomarker LHGDN our results suggest that eNOS gene may have gender-specific and age-dependent effects on DBP and the development of hypertension risk. 16041245

2005

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Associations of the angiotensin II type 1 receptor A1166C and the endothelial NO synthase G894T gene polymorphisms with silent subcortical white matter lesions in essential hypertension. 16109907

2005

Entrez Id: 3291
Gene Symbol: HSD11B2
HSD11B2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 AlteredExpression LHGDN Variable activity of 11 beta HSD2 is relevant for blood pressure control and hypertension. 15489962

2004

Entrez Id: 3291
Gene Symbol: HSD11B2
HSD11B2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 AlteredExpression LHGDN Impaired 11-beta hydroxysteroid dehydrogenase type 2 activity in sweat gland ducts in human essential hypertension. 14981055

2004

Entrez Id: 3291
Gene Symbol: HSD11B2
HSD11B2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 Biomarker LHGDN The decreased activity of 11beta-HSD2 increases the intracellular availability of cortisol, which might be relevant for the pathogenesis of hypertension and preeclampsia. 12911547

2003

Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Peroxisome proliferator-activated receptor gamma C161T polymorphisms and survival of Japanese patients with immunoglobulin A nephropathy. 14616762

2003

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN [NOS3 gene polymorphism and left ventricular hypertrophy in patients with essential hypertension]. 12494183

2002

Entrez Id: 335
Gene Symbol: APOA1
APOA1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN Apolipoprotein AI promoter variant in blood pressure determination. 12030900

2002

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation LHGDN The endothelial nitric oxide synthase Glu298Asp polymorphism has been suggested to play a role in the development of hypertension, atherosclerosis and coronary artery disease. 12359981

2002

Entrez Id: 1889
Gene Symbol: ECE1
ECE1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.630 GeneticVariation LHGDN We genotyped 5 single nucleotide polymorphisms (SNPs) in the ECE1 gene in 1,873 individuals from a general Japanese population and identified one SNP associated with hypertension in women (rs212528: TT vs. TC+CC: odds ratio=1.40; 95% confidence intervals: 1.04-1.89; p=0.026), after adjusting for confounding factors. 17664854

2007