Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004096
Disease: Asthma
Asthma
0.180 GeneticVariation disease BEFREE The purpose of this study was to explore the relationship between NOD2 gene polymorphisms and asthma susceptibility in the Chinese Han population. 30950247 2019
CUI: C0004096
Disease: Asthma
Asthma
0.180 GeneticVariation disease GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
CUI: C0004096
Disease: Asthma
Asthma
0.180 AlteredExpression disease BEFREE NOD2 mRNA relative expression levels were significantly decreased in atopic asthmatic cases relative to controls with lower values among severe atopic asthmatics. 29572197 2018
CUI: C0004096
Disease: Asthma
Asthma
0.180 Biomarker disease BEFREE Taken together, our results indicate that NOD2 could serve as a potential diagnostic biomarker and therapeutic option for human asthma in the near future. 27889082 2017
CUI: C0004096
Disease: Asthma
Asthma
0.180 AlteredExpression disease BEFREE The new susceptibility region for TAO at 16q12 harbors variants that correlate with the expression of CYLD and nucleotide-binding oligomerization domain 2 (NOD2), 2 strong candidates for asthma. 27130862 2016
CUI: C0004096
Disease: Asthma
Asthma
0.180 AlteredExpression disease BEFREE Polymorphisms in the identified chitin receptors, NOD2 and TLR9, predispose individuals to inflammatory conditions and dysregulated expression of chitinases and chitinase-like binding proteins, whose activity is essential to generate IL-10-inducing fungal chitin particles in vitro, have also been linked to inflammatory conditions and asthma. 24722226 2014
CUI: C0004096
Disease: Asthma
Asthma
0.180 AlteredExpression disease BEFREE The situation is complicated further by the fact that WT NOD2 and WT RIP2 activity has been implicated in diseases such as asthma, inflammatory arthritis and MS. 23794710 2013
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
CUI: C0004096
Disease: Asthma
Asthma
0.180 GeneticVariation disease BEFREE In addition, a CARD15 haplotype revealed to be protective against the development of asthma (OR=0.326, P=0.003). 16008671 2005
CUI: C0004096
Disease: Asthma
Asthma
0.180 GeneticVariation disease BEFREE We genotyped a large population of German schoolchildren (N = 1872) from East and West Germany for 3 functional relevant CARD15 polymorphisms for their role in the development of asthma and allergy. 12704363 2003
CUI: C0004096
Disease: Asthma
Asthma
0.180 Biomarker disease HPO