Disease: Pediatric Crohn's disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		0.070 GeneticVariation disease BEFREE We hypothesized that concurrent GM-CSF Ab and CARD15 risk allele carriage (C15(+) GMAb(+) ) would be associated with growth failure in CD and growth hormone (GH) resistance in murine ileitis. 21337672 2012
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		0.070 GeneticVariation disease BEFREE NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease. 20713205 2010
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		0.070 AlteredExpression disease BEFREE Mucosal NOD2 expression and NF-kappaB activation in pediatric Crohn's disease. 18092345 2008
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		0.070 GeneticVariation disease BEFREE Polymorphisms 3020insC in CARD15 and SNP rs3792876 in SLC22A4/5 occurred statistically significantly more often in patients with pediatric-onset CD than in patients with adult-onset CD. 17476680 2007
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		0.070 GeneticVariation disease BEFREE CARD15 mutations are rare in Swedish pediatric Crohn disease. 15795594 2005
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		0.070 GeneticVariation disease BEFREE The authors found a nonsignificant trend of a lower body mass index and higher Pediatric Crohn Disease Activity Index in patients with CARD15 mutations. 15990626 2005
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		0.070 GeneticVariation disease BEFREE CARD15 gene mutations and risk for early surgery in pediatric-onset Crohn's disease. 15551253 2004