Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease BEFREE The aim of this study was to investigate the relationship of <i>TLR1, TLR6, MYD88</i> and <i>TIRAP</i> polymorphisms with susceptibility to latent tuberculosis infection (LTBI) and tuberculosis (TB). 30963003 2019
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 Biomarker disease BEFREE To test common and rare TLR variants involved in susceptibility or resistance to infection with Mycobacterium tuberculosis we screened the exons of the genes encoding TLR 1, 2, 4, and the adaptor molecule TIRAP in more than 4500 tuberculosis (TB) cases and controls from Ghana. 27214039 2016
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease BEFREE Humans that are heterozygous for the common S180L polymorphism in the Toll-like receptor (TLR) adaptor Mal (encoded by TIRAP) are protected from a number of infectious diseases, including tuberculosis (TB), whereas those homozygous for the allele are at increased risk. 26885859 2016
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease BEFREE Coinheritance of these polymorphisms with previously identified risk alleles in Toll-like receptor 2 and TIRAP was associated with an additive risk of tuberculosis susceptibility. 22223854 2012
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease BEFREE We investigated all the single-nucleotide polymorphisms (SNPs) within the TIRAP exon 5 in a case-control study of 212 patients with tuberculosis and 215 controls in a Chinese population. 21218381 2011
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease BEFREE Polymorphisms in TIRAP do not appear to be involved in childhood TB susceptibility in South Africa, but may play a role in determining occurrence of TBM. 19693265 2009
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease BEFREE These results support the influence of TIRAP (MAL) S180L polymorphism on TB and indicate that TB and SLE might share a common immunogenetic pathway in the innate immune response. 18417424 2008
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease LHGDN Analysis of association of the TIRAP (MAL) S180L variant and tuberculosis in three populations. 18305471 2008
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 GeneticVariation disease LHGDN These results support the influence of TIRAP (MAL) S180L polymorphism on TB and indicate that TB and SLE might share a common immunogenetic pathway in the innate immune response. 18417424 2008
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.380 Biomarker disease CTD_human A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis. 17322885 2007
CUI: C0024530
Disease: Malaria
Malaria
0.330 GeneticVariation disease BEFREE MyD88-adaptor-like/TIR domain containing adaptor protein polymorphism for single nucleotide polymorphism rs8177374 is related with the susceptibility of malaria. 28482182 2017
CUI: C0024530
Disease: Malaria
Malaria
0.330 Biomarker disease BEFREE Genetic polymorphisms (SNPs) in different TLRs, TIRAP, and CD14 were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis in 325 patients infected with P. vivax and 274 healthy individuals without malaria history in the prior 12 months from the same endemic area.Parasite load was determined by qPCR. 28850598 2017
CUI: C0024530
Disease: Malaria
Malaria
0.330 GeneticVariation disease BEFREE A mutation (S180L) in the TLR downstream signal transducer TIRAP has recently been reported to be common in Europeans and Africans and to roughly half the risks of heterogeneous infectious diseases including malaria, tuberculosis, bacteremia, and invasive pneumococal disease in heterozygous mutation carriers. 19602285 2009
CUI: C0024530
Disease: Malaria
Malaria
0.330 Biomarker disease CTD_human A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis. 17322885 2007
CUI: C0004610
Disease: Bacteremia
Bacteremia
0.300 Biomarker disease CTD_human A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis. 17322885 2007
CUI: C0032269
Disease: Pneumococcal Infections
Pneumococcal Infections
0.300 Biomarker group CTD_human A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis. 17322885 2007
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
0.300 Biomarker group CTD_human The interaction of four genes in the inflammation pathway significantly predicts prostate cancer risk. 16284379 2005
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.300 Biomarker disease CTD_human The interaction of four genes in the inflammation pathway significantly predicts prostate cancer risk. 16284379 2005
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)
0.300 Biomarker disease CTD_human
Invasive Pneumococcal Disease, Recurrent Isolated, 1
0.300 Biomarker disease CTD_human
Low density lipoprotein cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
High density lipoprotein measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012