Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.600 GeneticVariation LHGDN In conclusion, our findings indicate that the -A2843G polymorphism in the ANP gene promoter might be a genetic risk factor for the development of LVH in patients with hypertension. 17672826

2008

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.600 GeneticVariation LHGDN In this cohort, the ANP gene variant was associated with early blood pressure increase and predisposition to develop hypertension. 17525707

2007

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.600 Biomarker LHGDN If corroborated by other large-scale, prospective studies, our findings indicate that the natriuretic peptide precursor A gene plays a significant role in blood pressure regulation and development of hypertension. 17984371

2007

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.600 Biomarker LHGDN The concentration of atrial and brain natriuretic peptide in patients with idiopathic hypertension. 17901852

2007

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.600 Biomarker LHGDN Association of atrial natriuretic peptide and type a natriuretic peptide receptor gene polymorphisms with left ventricular mass in human essential hypertension. 16875975

2006

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.570 Biomarker LHGDN N-terminal pro-atrial natriuretic peptide and exercise prescription in patients with myocardial infarction. 17292492

2007

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.570 GeneticVariation LHGDN According to our knowledge, this study is the first to look for the potential association of the ScaI ANP gene polymorphism with the history of nonfatal myocardial infarction and the extent of coronary artery disease (CAD). 12514664

2003

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.560 GeneticVariation LHGDN Atrial natriuretic peptide gene promoter polymorphism is associated with left ventricular hypertrophy in hypertension. 17672826

2008

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.560 Biomarker LHGDN The concentration of atrial and brain natriuretic peptide in patients with idiopathic hypertension. 17901852

2007

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.520 Biomarker LHGDN Atrial natriuretic peptide and CD34 overexpression in human idiopathic dilated cardiomyopathies. 18092954

2007

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
0.230 Biomarker LHGDN Neurohumoral profiles in patients with hypertrophic cardiomyopathy: differences to hypertensive left ventricular hypertrophy. 15118286

2004

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.200 GeneticVariation LHGDN Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation. 18614783

2008

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.200 GeneticVariation LHGDN Atrial natriuretic peptide gene polymorphisms and risk of ischemic stroke in humans. 15017020

2004

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.040 GeneticVariation LHGDN To test whether participants with minor NPPA alleles in the T2238C or G664A variants had different rates of cardiovascular disease or blood pressure (BP) changes than common allele homozygotes when treated with a diuretic vs other antihypertensive medications. 18212314

2008

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
0.020 Biomarker LHGDN N-terminal pro A-type natriuretic peptide but not N-terminal pro C-type natriuretic peptide concentrations are related to cardiac diseases in infants. 18280250

2008

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0004096
Disease: Asthma
Asthma
0.010 GeneticVariation LHGDN Determine associations between asthma and four common SNPs on the NPPA gene: C/G (rs13305986) in the promoter; G/A (rs5063) in Exon 1 resulting in NPPAMet32-->Val substitution; T/C (rs5065) in Exon 3 resulting in an Arg152-->Ter substitution; and T/C in the 3'UT region (rs5067). 18294255

2008

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0026266
Disease: Mitral Valve Insufficiency
Mitral Valve Insufficiency
0.010 AlteredExpression LHGDN Severe mitral regurgitation-relations between magnetic resonance imaging, echocardiography and natriuretic peptides. 17943627

2008

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial
0.010 AlteredExpression LHGDN Natriuretic peptide Val7Met substitution and risk of coronary artery disease in Greek patients with familial hypercholesterolemia. 16721833

2006

Entrez Id: 4878
Gene Symbol: NPPA
NPPA
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.010 Biomarker LHGDN Increased plasma levels of natriuretic peptide type B and A in children with congenital heart defects with left compared with right ventricular volume overload or pressure overload. 16117728

2005