Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Apolipoprotein E (APOE) E4, apolipoprotein B-100 (APOB) Q3611 allele, the angiotensin converting enzyme (ACE) deletion (D) allele and glycoprotein IIIa (GP3A) P33 mutant allele are reported to predispose to early-onset coronary heart disease (CHD). 10463820 1999
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE In the present study, a cross-sectional analysis was performed to evaluate the potential relationship between the ACE I/D genotypes and the LV mass index in 289 non-insulin-dependent diabetes mellitus (NIDDM) subjects without known coronary artery disease. 10371375 1999
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Thus, our study suggests that genetic polymorphisms of angiotensin-converting enzyme insertion/deletion are associated with in-stent restenosis in coronary artery disease patients following coronary stenting. 28196432 2017
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE In association analysis the ACE genotype frequencies of probands with CHD did not differ from those of healthy controls. 11427204 2001
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE We have tested the hypothesis that the angiotensin-converting enzyme (ACE) DD genotype and the angiotensin II type I receptor (AT1R) gene C allele represent the common link between microalbuminuria and coronary heart disease. 9351388 1997
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE A multiple logistic regression analysis introducing the typical risk factors for CHD (age, gender, smoking, BMI > 26 kg/m 2, LDL elevation, HbA1c > 7 %) could not identify the ACE gene I/D-polymorphism as an independent risk factor for CHD (p = 0.87). 12669270 2003
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The presence of deletion (D) allele in angiotensin converting enzyme (ACE) gene polymorphism is associated with coronary artery disease. 17285438 2007
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The present results show that subjects with the ACE/DD genotype are not at increased risk for CHD because of insulin resistance, relative hyperglycemia and hyperinsulinemia, or a dyslipidemia characterized by a high triglyceride and low HDL cholesterol concentration.(ABSTRACT TRUNCATED AT 250 WORDS) 7773733 1995
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Association of angiotensin-converting enzyme polymorphism with coronary artery disease in Iranian patients with unipolar depression. 22683751 2012
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE It has been suggested that the insertion (I)/deletion (D) polymorphism of the angiotensin-converting enzyme (ACE) gene is an independent risk factor for coronary artery disease, but its relation to stroke has not yet been proven. 8784123 1996
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The aim of this study was to determine whether the angiotensin-converting enzyme (ACE) insertion-deletion (ID) polymorphism interacts with pravastatin to modify the risk of coronary heart disease (CHD) and other cardiovascular end points in a large clinical trial. 17174637 2007
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The angiotensin converting enzyme D allele is an independent risk factor for early onset coronary artery disease. 20655894 2010
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Considering the possible interaction between this polymorphism and smoking, we evaluated the association between ACE I/D polymorphism and myocardial infarction (MI), mortality due to coronary heart disease (CHD), and cardiovascular disease (CVD). 15635071 2005
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE By contrast, there was no evidence of a significant increase in the risk of CHD or myocardial infarction among individuals with ACE DD. 7783537 1995
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE ACE insertion/deletion gene polymorphism is associated neither with the prevalence nor the extent of coronary artery disease, nor with myocardial infarction in this relatively large sample of Caucasian men and women. 10462466 1999
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Our report indicates the increased risk of coronary artery disease in the presence of ACE DD and AT1R CC genotypes independent of other risk factors, in Italian patients. 10731400 2000
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Tetra primer ARMS-PCR relates folate/homocysteine pathway genes and ACE gene polymorphism with coronary artery disease. 21567207 2011
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The ACE/ID polymorphism seems to be a potent risk factor of coronary heart disease in subjects formerly considered to be at low risk according to common criteria. 1328889 1992
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE A meta-analysis assessing the influence of the ACE polymorphism on disease susceptibility demonstrated significant odds ratios in individuals with the DD genotype for coronary heart disease, myocardial infarction and both diabetic and nondiabetic renal disease. 10391391 1999
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Recently, attention has been focused on the correlation between coronary artery disease and genetic factors, such as ACE gene polymorphism or the gene polymorphism for the IIIa-moiety of the platelet fibrinogen receptor IIb-IIIa. 9519344 1998
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Many authors have reported an association between the angiotensin-converting enzyme (ACE)-D allele and coronary heart disease and other cardiovascular diseases. 10765051 2000
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Angiotensin-converting enzyme insertion/deletion gene polymorphic variant as a marker of coronary artery disease: a meta-analysis. 18504336 2008
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677-->T transition in the MTHFR gene. 12833177 2003
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Left ventricular size, mass and function in relation to angiotensin-converting enzyme gene and angiotensin-II type 1 receptor gene polymorphisms in patients with coronary artery disease. 12747597 2003
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Traditional risk factors and angiotensin-converting enzyme insertion/deletion gene polymorphism in coronary artery disease. 25867352 2015