Source: GWASDB ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669 2013
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388 2012
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966 2010
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756 2007
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. 17447842 2007
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB A proportion of these were replicated in two independent German Caucasian samples, including the established CD loci NOD2 and IBD5. 17804789 2007
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544 2007
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300 2007
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation disease GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223 2006
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.500 GeneticVariation group GWASDB Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. 18758464 2008
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.500 GeneticVariation group GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223 2006
CUI: C0004096
Disease: Asthma
Asthma 		0.180 GeneticVariation disease GWASDB Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. 21150878 2011