VWF, von Willebrand factor, 7450

N. diseases: 498; N. variants: 158
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010051
Disease: Coronary Aneurysm
Coronary Aneurysm
0.010 Biomarker disease BEFREE The vWF:Collagen binding activity/vWF:Antigen ratio, however, was significantly decreased in patients with a coronary artery lesion (z-score > 2; N = 10; mean ratio 0.96 vs. 0.64; p = 0.031) and even more so in those with a coronary artery aneurysm (z-score > 2.5; N = 8; mean ratio 0.94 vs. 0.55; p = 0.02). 31760507 2020
Disseminated Intravascular Coagulation
0.010 AlteredExpression disease BEFREE In patients with S. aureus bloodstream infections, high VWF levels and low ADAMTS13 activity levels correlated with disease severity and with parameters of inflammation and disseminated intravascular coagulation (DIC). 31758651 2020
CUI: C0151798
Disease: Hepatic necrosis
Hepatic necrosis
0.010 AlteredExpression phenotype BEFREE VWF plasma levels were measured by ELISA, and liver necrosis or hepatocyte proliferation was measured by immunohistochemistry. 31606553 2020
CUI: C1290884
Disease: Inflammatory disorder
Inflammatory disorder
0.010 Biomarker group BEFREE The association of Kawasaki disease, a vascular inflammatory disease and vWF:Antigen, vWF:Collagen binding activity, and vWF multimers is unknown. 31760507 2020
CUI: C2609079
Disease: Mirror syndrome
Mirror syndrome
0.010 Biomarker disease BEFREE Notably, we elucidated a temporal spectrum of maternal serum mediators (soluble Flt-1, endothelin-1, 8-isoprostane, activin-A, ICAM-1, and vWF) involved in the pathogenesis of Mirror syndrome. 30614331 2020
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
0.010 GeneticVariation disease BEFREE In particular, non-random occurrence was revealed for SERPINA1 c.1096G > A (alpha-1 antitrypsin deficiency), C8B c.1282C > T and c.1653G > A (complement component 8B deficiency), ATP7B c.3207C > A (Wilson disease), PROP1 c.301_302delAG (combined pituitary hormone deficiency), CYP21A2 c.844G > T (non-classical form of adrenogenital syndrome), EYS c.1155T > A (retinitis pigmentosa), HADHA c.1528G > C (LCHAD deficiency), SCO2 c.418G > A (cytochrome c oxidase deficiency), OTOA c.2359G > T (sensorineural deafness), C2 c.839_866del (complement component 2 deficiency), ACADVL c.848T > C (VLCAD deficiency), TGM5 c.337G > T (acral peeling skin syndrome) and VWF c.2561 G > A (von Willebrand disease, type 2N). 31028847 2019
CUI: C0002873
Disease: Anemia of chronic disease
Anemia of chronic disease
0.010 GeneticVariation phenotype BEFREE In the present review, we focus on aptamers as potential therapeutics for hematological diseases, including anemia of chronic inflammation (ACI) and anemia of chronic disease (ACD), hemophilia, thrombotic thrombocytopenic purpura (TTP) or VWD type-2B, and sickle cell disease (SCD), in particular, those that have entered into clinical trials. 28969551 2019
CUI: C0002965
Disease: Angina, Unstable
Angina, Unstable
0.010 AlteredExpression disease BEFREE Serum PTX-3, vWf and CXCL13 levels were significantly higher in USAP group than those in either SAP or control groups (p˂0.001). 31066256 2019
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.010 Biomarker disease BEFREE These results suggest that GLA deficiency promotes VWF secretion through eNOS dysregulation, which may contribute to the vasculopathy of Fabry disease. 30470436 2019
CUI: C0003864
Disease: Arthritis
Arthritis
0.010 Biomarker disease BEFREE Moreover, interleukin (IL)-1β and vascular endothelial growth factor (VEGF) levels were reduced, and fewer von Willebrand factor (vWF)-stained areas were identified in the fullerenol-treated joints than in control joints.The i.a. injection of fullerenol for reducing ROS production can ameliorate arthritis in joints by suppressing pro-inflammatory cytokine production and the angiogenesis process.Thus, the i.a. injection of fullerenol for reducing the production of ROS can be used as a pharmacological approach for RA patients. 31234583 2019
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
0.010 Biomarker disease BEFREE Increased von Willebrand factor parameters in children with febrile seizures. 30605489 2019
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
0.010 AlteredExpression disease BEFREE In contrast, the VD group showed increased fibrinogen levels (SMD: 0.77; 95% CI: 0.13-1.41), activated factor VII (SMD: 0.36; 95% CI: 0.05-0.67), factor VIII (SMD: 0.57; 95% CI: 0.22-0.91), VWF (SMD: 2.34; 95% CI: 0.38-4.29), D-dimer (SMD: 1.14; 95% CI: 0.51-1.78), and homocysteine (SMD: 2.17; 95% CI: 1.67-2.68). 31096308 2019
CUI: C0011311
Disease: Dengue Fever
Dengue Fever
0.010 Biomarker disease BEFREE Desialylation of platelets induced by Von Willebrand Factor is a novel mechanism of platelet clearance in dengue. 30849118 2019
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus
0.010 Biomarker disease BEFREE Five decreased proteins (platelet factor 4, fibrinogen, von Willebrand factor, collagen, and mannose binding lectin-associated serine protease-2) and one increased protein (fibronectin) may increase the risk of patent ductus arteriosus. 30480800 2019
CUI: C0014867
Disease: Esophageal Varices
Esophageal Varices
0.010 AlteredExpression disease BEFREE Levels of vEF were correlated positively with esophageal varices grade. 30281535 2019
CUI: C0017145
Disease: Gastric Varix
Gastric Varix
0.010 AlteredExpression disease BEFREE <b>Methods:</b> The results of impedance aggregometry, von Willebrand factor antigen level and thromboelastometry (TEM) with and without the addition of a platelet inhibitor (FIBTEM<sup>®</sup>, EXTEM<sup>®</sup> test, respectively) were compared in two patient groups: Group 1 (<i>n</i> = 32) - patients with moderate or large esophageal or gastric varices, who had never had symptoms of acute gastrointestinal bleeding and Group 2 (<i>n</i> = 26) - patients with history of variceal bleeding. 30907172 2019
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.010 AlteredExpression disease BEFREE Proper hematological investigations before glaucoma surgery in the left eye revealed a low level of factor VIII with normal levels of factor IX and von Willebrand's factor antigen. 30938185 2019
CUI: C0018524
Disease: Hallucinations
Hallucinations
0.010 AlteredExpression disease BEFREE We used biochemical methods to assess microvessel density (level of von Willebrand factor, a marker of endothelial cell content), ante-mortem oxygenation (vascular endothelial growth factor, a marker of tissue hypoxia; myelin-associated glycoprotein to proteolipid protein-1 ratio, a measure of tissue oxygenation relative to metabolic demand), cholinergic innervation (acetylcholinesterase and choline acetyltransferase), butyrylcholinesterase and insoluble α-synuclein content in the BA18 and BA19 occipital cortex obtained post-mortem from 23 AD patients who had experienced visual hallucinations, 19 AD patients without hallucinations, 19 DLB patients, and 36 controls. 31511061 2019
Sensorineural Hearing Loss (disorder)
0.010 GeneticVariation disease BEFREE In particular, non-random occurrence was revealed for SERPINA1 c.1096G > A (alpha-1 antitrypsin deficiency), C8B c.1282C > T and c.1653G > A (complement component 8B deficiency), ATP7B c.3207C > A (Wilson disease), PROP1 c.301_302delAG (combined pituitary hormone deficiency), CYP21A2 c.844G > T (non-classical form of adrenogenital syndrome), EYS c.1155T > A (retinitis pigmentosa), HADHA c.1528G > C (LCHAD deficiency), SCO2 c.418G > A (cytochrome c oxidase deficiency), OTOA c.2359G > T (sensorineural deafness), C2 c.839_866del (complement component 2 deficiency), ACADVL c.848T > C (VLCAD deficiency), TGM5 c.337G > T (acral peeling skin syndrome) and VWF c.2561 G > A (von Willebrand disease, type 2N). 31028847 2019
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute
0.010 Biomarker disease BEFREE To test this hypothesis, we studied the role of VWF in AKI using a mouse model of acute ischemia-reperfusion (I/R) kidney injury. 31594992 2019
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia
0.010 Biomarker disease BEFREE Considering vWF and ADAMTS-13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) as markers of endothelial dysfunction and activation, we evaluated the prognostic importance of vWF and ADAMTS-13 antigen levels in the serum of patients with previously untreated symptomatic WM to validate vWF as a possible prognostic marker for progression-free and overall survival. 30224328 2019
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.010 AlteredExpression disease BEFREE In MFS von Willebrand factor (VWF) activity (81.9%±41.8% <i>vs.</i> 106.3%±41.5%, P<0.05) and antigen (93.8%±43.9% <i>vs.</i> 118.8%±47.8%, P<0.05) and factor VIII activity (108.9%±29.6% <i>vs.</i> 126.7%±28.4%, P<0.05) were reduced. 31737529 2019
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.010 Biomarker disease BEFREE The aim of this study was to measure the concentrations of serum levels of vascular endothelial growth factor, D-dimer, and von Willebrand factor in patients with newly diagnosed or relapsed multiple myeloma before treatment, during therapy, and after successful therapy. 30845824 2019
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases
0.010 Biomarker group BEFREE Endothelial surface and circulating glycoprotein von Willebrand factor (vWF) regulates platelet adhesion and is associated with thrombotic diseases, including ischemic stroke, myocardial infarction, and peripheral vascular disease. 30987839 2019
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block
0.010 Biomarker disease BEFREE ETV treatment resulted in an increased ADAMTS13: AC and decreased VWF: Ag (both P < 0.001) in CHB patients. 30976044 2019