Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.400 Biomarker disease CTD_human A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570 2013
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.400 GeneticVariation disease GWASDB Genome-wide association study of susceptibility loci for cervical cancer. 23482656 2013
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.400 GeneticVariation disease GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570 2013
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		0.300 Biomarker disease CTD_human A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570 2013
CUI: C0005138
Disease: Berylliosis
Berylliosis 		0.300 Biomarker disease CTD_human Beryllium presentation to CD4+ T cells is dependent on a single amino acid residue of the MHC class II beta-chain. 16272364 2005
CUI: C2350873
Disease: Beryllium Disease
Beryllium Disease 		0.300 Biomarker disease CTD_human Beryllium presentation to CD4+ T cells is dependent on a single amino acid residue of the MHC class II beta-chain. 16272364 2005
CUI: C0004096
Disease: Asthma
Asthma 		0.100 GeneticVariation disease GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation phenotype GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.100 GeneticVariation disease GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.100 GeneticVariation disease GWASCAT Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. 25305756 2014
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.100 GeneticVariation disease GWASCAT Genome-wide association study of susceptibility loci for cervical cancer. 23482656 2013
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.100 GeneticVariation disease GWASDB A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. 21750111 2011
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.100 GeneticVariation group GWASCAT Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633 2011
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633 2011
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.100 GeneticVariation disease GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088 2009
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 Biomarker disease BEFREE Furthermore, heterozygous deletions overlapping the CFHR4, CFHR5 and HLA-DPB2 genes were described for the first time in SLE patients. 30485348 2018
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 GeneticVariation disease BEFREE The confirmatory studies in US Caucasians indicate that specific SNPs of HLA-DPB1 and/or DPB2 are strongly associated with US Caucasian patients with SSc who are positive for anti-DNA topoisomerase I or anticentromere autoantibodies. 19950302 2009
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 GeneticVariation disease BEFREE Finally, we tested these 24 SNPs in a third study (475 cases and 619 controls) and found that 5 SNPs in 4 genes (ENO1, FXN (2 SNPs), HLA-DPB2, and LPA) were associated with MI in the third study (1-sided P<0.05), and had the same risk alleles in all three studies. 18682748 2008