NPPA, natriuretic peptide A, 4878

N. diseases: 217; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.600 Biomarker group MGD
CUI: C1838539
Disease: CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE 		0.600 Biomarker disease HPO
CUI: C1838539
Disease: CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE 		0.600 Biomarker disease CTD_human
CUI: C2677294
Disease: Atrial Fibrillation, Familial, 6
Atrial Fibrillation, Familial, 6 		0.400 Biomarker disease CTD_human
CUI: C2677294
Disease: Atrial Fibrillation, Familial, 6
Atrial Fibrillation, Familial, 6 		0.400 CausalMutation disease CLINVAR
CUI: C3810401
Disease: ATRIAL STANDSTILL 2
ATRIAL STANDSTILL 2 		0.400 CausalMutation disease CLINVAR
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.200 Biomarker disease HPO
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.200 Biomarker group HPO
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.120 Biomarker group HPO
CUI: C0008767
Disease: Cicatrization
Cicatrization 		0.100 Biomarker phenotype HPO
CUI: C0013404
Disease: Dyspnea
Dyspnea 		0.100 Biomarker phenotype HPO
CUI: C0030252
Disease: Palpitations
Palpitations 		0.100 Biomarker phenotype HPO
CUI: C0085611
Disease: Atrial arrhythmia
Atrial arrhythmia 		0.100 Biomarker phenotype HPO
CUI: C0428977
Disease: Bradycardia
Bradycardia 		0.100 Biomarker phenotype HPO
CUI: C3160712
Disease: Palpitations, CTCAE
Palpitations, CTCAE 		0.100 Biomarker phenotype HPO
CUI: C4021885
Disease: Atrial cardiomyopathy
Atrial cardiomyopathy 		0.100 Biomarker disease HPO
CUI: C4025638
Disease: Hyperpepsinogenemia I
Hyperpepsinogenemia I 		0.100 Biomarker disease HPO
CUI: C4476545
Disease: Dilatation of the ventricular cavity
Dilatation of the ventricular cavity 		0.100 Biomarker phenotype HPO
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		0.300 Biomarker disease CTD_human Atrial natriuretic peptide in the diagnosis of patent ductus arteriosus. 1421905 1992
CUI: C2936170
Disease: Patent Ductus Arteriosus Familial
Patent Ductus Arteriosus Familial 		0.300 Biomarker disease CTD_human Atrial natriuretic peptide in the diagnosis of patent ductus arteriosus. 1421905 1992
CUI: C2314896
Disease: Familial Atypical Mole Melanoma Syndrome
Familial Atypical Mole Melanoma Syndrome 		0.010 GeneticVariation disease BEFREE To date, no support for linkage of MLM alone to these markers has been found; likewise no study has been able to exclude the entire region between PND and D1S47 from linkage to MLM. 1531137 1992
CUI: C0018801
Disease: Heart failure
Heart failure 		0.600 AlteredExpression disease BEFREE Previous studies have indicated that the serum level and ventricular expression of the ANP gene were augmented in patients with heart failure. 1535030 1992
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.600 AlteredExpression disease BEFREE Previous studies have indicated that the serum level and ventricular expression of the ANP gene were augmented in patients with heart failure. 1535030 1992
CUI: C0018801
Disease: Heart failure
Heart failure 		0.600 Biomarker disease CTD_human Mechanisms of sodium retention in heart failure: relation to the renin-angiotensin-aldosterone system. 1647690 1991
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.600 Biomarker disease CTD_human Mechanisms of sodium retention in heart failure: relation to the renin-angiotensin-aldosterone system. 1647690 1991