Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 Biomarker disease BEFREE Vigilin, a nucleocytoplasmic shuttling protein, post-transcriptionally suppresses proto-oncogene c-fms expression (encoding CSF-1R) in breast cancer by binding to a 69 nt cis-acting 3-UTR element in CSF-1R mRNA. 30292064 2019
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 AlteredExpression disease BEFREE Multidimensional analysis of microarray datasets demonstrated up-regulation of genes encoding HBP enzymes in clinical breast cancers and revealed that co-expression of hyaluronan synthase 2 (HAS2) and glutamine:fructose-6-phosphate amidotransferase (GFAT), a rate-limiting enzyme of the HBP, was strongly correlated with a poor prognosis in advanced cancer patients. 31645543 2019
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 Biomarker disease BEFREE In summary, we identified a competition for binding the 69-nt sequence, through which vigilin and HuR exert opposing effects on c-fms expression, suggesting a role for vigilin in suppression of breast cancer progression. 20974809 2011
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 GeneticVariation disease UNIPROT
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.310 GeneticVariation disease BEFREE FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome. 19365831 2009
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.310 Biomarker disease CTD_human FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome. 19365831 2009
CUI: C2931817
Disease: Chromosome 2q37 deletion syndrome
Chromosome 2q37 deletion syndrome
0.300 Biomarker disease CTD_human FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome. 19365831 2009
CUI: C0005890
Disease: Body Height
Body Height
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0040420
Disease: Tonometry
Tonometry
0.100 GeneticVariation phenotype GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
CUI: C0037369
Disease: Smoking
Smoking
0.100 GeneticVariation phenotype GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.100 GeneticVariation phenotype GWASCAT Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. 28107422 2017
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
0.100 GeneticVariation phenotype GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.100 GeneticVariation disease GWASCAT Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. 26956414 2016
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.100 GeneticVariation phenotype GWASCAT A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. 26561523 2016
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
0.100 GeneticVariation disease GWASCAT Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. 26956414 2016
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.100 GeneticVariation disease GWASDB Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.050 Biomarker disease BEFREE Home blood pressure is associated with cognitive impairment among elderly patients with type 2 diabetes: KAMOGAWA-HBP study. 31081363 2019
Diabetes Mellitus, Non-Insulin-Dependent
0.050 Biomarker disease BEFREE Isolated high home systolic blood pressure in patients with type 2 diabetes is a prognostic factor for the development of diabetic nephropathy: KAMOGAWA-HBP study. 31711859 2019
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.050 Biomarker disease BEFREE Maximum morning home systolic blood pressure is an indicator of the development of diabetic nephropathy: The KAMOGAWA-HBP study. 30884176 2019
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.050 Biomarker disease BEFREE Isolated high home systolic blood pressure in patients with type 2 diabetes is a prognostic factor for the development of diabetic nephropathy: KAMOGAWA-HBP study. 31711859 2019
Diabetes Mellitus, Non-Insulin-Dependent
0.050 Biomarker disease BEFREE Impact of masked hypertension on diabetic nephropathy in patients with type II diabetes: a KAMOGAWA-HBP study. 29548933 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.050 Biomarker disease BEFREE Threshold value of home pulse pressure predicting arterial stiffness in patients with type 2 diabetes: KAMOGAWA-HBP study. 29447439 2018
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.050 Biomarker disease BEFREE Impact of masked hypertension on diabetic nephropathy in patients with type II diabetes: a KAMOGAWA-HBP study. 29548933 2018
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.050 Biomarker disease BEFREE Prognostic significance of home pulse pressure for progression of diabetic nephropathy: KAMOGAWA-HBP study. 29540826 2018