Disease: IIeocolitis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human NOD2-associated diseases: Bridging innate immunity and autoinflammation. 19467619 2010
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. 18438406 2008
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human NOD2/CARD15 gene variants are linked to failure of antibiotic treatment in perianal fistulating Crohn's disease. 18371140 2008
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 GeneticVariation disease BEFREE Analysis of 229 patients with ileal or ileocolonic disease and a NOD2/CARD15 mutation disclosed that ileocolitis was more prevalent through age 10, while isolated ileitis was more prevalent above age 10 (P = 0.016). 17763471 2007
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human Cell culture models in developing nutrigenomics foods for inflammatory bowel disease. 17568627 2007
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756 2007
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 GeneticVariation disease BEFREE Regarding the location of the disease, the concomitant presence of the TC haplotype and NOD2/CARD15 mutations was mainly associated with ileocolitis or ileitis. 16437728 2005
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 GeneticVariation disease BEFREE The NOD2/CARD15 mutations are risk factors for CD in Greece, they appear to predict an earlier age of onset and are associated particularly with ileitis or ileocolitis. 15489579 2004
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human CARD15 mutations in Blau syndrome. 11528384 2001
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. 11385577 2001
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.330 Biomarker disease CTD_human Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. 11385576 2001