Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE Loss-of-function CARD8 mutation causes NLRP3 inflammasome activation and Crohn's disease. 29408806 2018
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE However, subgroup analysis based on different CD types showed a significant association between the CARD8 polymorphism and CD risk in the additive model (ileal CD: OR = 0.83, 95% CI = 0.70-0.98; stenotic or fistulizing CD: OR = 0.81, 95% CI = 0.72-0.92). 26462578 2015
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE CARD8 gene variant is a risk factor for recurrent surgery in patients with Crohn's disease. 26283210 2015
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE The association between rs2043211" genes_norm="22900">p.C10X mutation (rs2043211) of the CARD8 gene and the levels of anti-glycans antibody response was examined in 39 CD families. 23506543 2013
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE Our data suggest that CARD8 variants might have roles in the pathogenesis of CD and UC in Koreans. 21248762 2011
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE Evidence of interaction of CARD8 rs2043211 with NALP3 rs35829419 in Crohn's disease. 20182451 2010
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE Our results show that men who have both the C10X and Q705K alleles in CARD8 and NALP3, and who express wild-type alleles of Nod2 are at an increased risk of developing CD (odds ratio, OR: 3.40 range: 1.32-8.76); P = 0.011). 19319132 2009
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE No association of the CARD8 (TUCAN) c.30T>A (p.C10X) variant with Crohn's disease: a study in 3 independent European cohorts. 18092344 2008
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease LHGDN We have shown an association between a likely functional polymorphism in TUCAN and CD. 17030188 2006
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.090 GeneticVariation disease BEFREE We have shown an association between a likely functional polymorphism in TUCAN and CD. 17030188 2006