Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206178
Disease: Cytomegalovirus Retinitis
Cytomegalovirus Retinitis
0.010 GeneticVariation disease BEFREE In European Americans (n = 750), a haplotype carrying an amino acid changing variation in the cytoplasmic domain (S420L) of IL-10R1 can be protective (OR, 0.14; 95% CI, 0.02-0.94; P = .04) against, whereas another haplotype carrying an amino acid changing variation in the extracellular domain (I224V) of IL-10R1 can be more susceptible (OR, 6.21; 95% CI, 1.22- 31.54; P = .03) to CMV retinitis. 20617924 2010