Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 GeneticVariation disease BEFREE Independent association genetic studies have implicated OLR1 gene variants in myocardial infarction (MI) susceptibility. 15976314 2005
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 Biomarker disease CTD_human Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 14684693 2003
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 Biomarker disease BEFREE The lectin-like oxidized LDL receptor LOX-1 (encoded by OLR1) is believed to play a key role in atherogenesis and some reports suggest an association of OLR1 polymorphisms with myocardial infarction (MI). 18384690 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 Biomarker disease CTD_human These findings suggest that OLR1 or a neighboring gene linked with G501C SNP is important for the incidence of MI. 12646194 2003
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 Biomarker disease BEFREE LOX-1 is increasingly viewed as a vascular disease biomarker and a potential therapeutic target in heart attack and stroke prevention. 18092947 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 Biomarker disease BEFREE The cardiac lectin-like oxidized low-density-lipoprotein receptor-1 is activated by oxidative stress in ischaemia-reperfusion injury, inducing apoptosis in cardiomyocytes through the deleterious NF-kB pathway, while the administration of anti-lectin-like oxidized low-density-lipoprotein receptor-1 antibody suppresses apoptosis and reduces the extent of myocardial infarction. 31782085 2020
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 SusceptibilityMutation disease CLINVAR
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 Biomarker disease LHGDN Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 14684693 2003
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 GeneticVariation disease BEFREE Recently, a 3'-UTR (188 C>T) SNP in the OLR1 gene has been reported to be associated with coronary artery stenosis and myocardial infarction. 16829343 2006
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 GeneticVariation disease BEFREE Recently, LOX-1 gene polymorphism (G501C) was reported to be associated with myocardial infarction (MI). 15562935 2004
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 GeneticVariation disease BEFREE In humans, LOX-1 gene polymorphisms were associated with increased susceptibility to myocardial infarction. 23935243 2013
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.490 GeneticVariation disease BEFREE These findings suggest that OLR1 or a neighboring gene linked with G501C SNP is important for the incidence of MI. 12646194 2003
CUI: C0018801
Disease: Heart failure
Heart failure
0.320 GeneticVariation disease BEFREE Deletion of LOX-1 Protects against Heart Failure Induced by Doxorubicin. 27195769 2016
CUI: C0018801
Disease: Heart failure
Heart failure
0.320 Biomarker disease CTD_human Vascular and thrombogenic effects of pulmonary exposure to Libby amphibole. 22352330 2012
CUI: C0018801
Disease: Heart failure
Heart failure
0.320 Biomarker disease BEFREE In conclusion, α1-antitrypsin and lectin-like oxidized low-density-lipoprotein receptor-1 seem to represent two good markers in HF and therapeutic targets, whereas galectin-3 does not. 31782085 2020
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.320 GeneticVariation disease BEFREE Deletion of LOX-1 Protects against Heart Failure Induced by Doxorubicin. 27195769 2016
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.320 Biomarker disease BEFREE In conclusion, α1-antitrypsin and lectin-like oxidized low-density-lipoprotein receptor-1 seem to represent two good markers in HF and therapeutic targets, whereas galectin-3 does not. 31782085 2020
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.320 Biomarker disease CTD_human Vascular and thrombogenic effects of pulmonary exposure to Libby amphibole. 22352330 2012
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure
0.300 Biomarker disease CTD_human Vascular and thrombogenic effects of pulmonary exposure to Libby amphibole. 22352330 2012
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease
0.300 Biomarker disease CTD_human Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets. 19565504 2009
CUI: C0235527
Disease: Heart Failure, Right-Sided
Heart Failure, Right-Sided
0.300 Biomarker disease CTD_human Vascular and thrombogenic effects of pulmonary exposure to Libby amphibole. 22352330 2012
CUI: C1959583
Disease: Myocardial Failure
Myocardial Failure
0.300 Biomarker disease CTD_human Vascular and thrombogenic effects of pulmonary exposure to Libby amphibole. 22352330 2012
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.300 Biomarker disease CTD_human Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets. 19565504 2009
CUI: C3714758
Disease: Juvenile psoriatic arthritis
Juvenile psoriatic arthritis
0.300 Biomarker disease CTD_human Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets. 19565504 2009
Polyarthritis, Juvenile, Rheumatoid Factor Negative
0.300 Biomarker disease CTD_human Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets. 19565504 2009