Gene: NOD2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.070 Biomarker disease BEFREE Autoinflammatory disease with focus on NOD2-associated disease in the era of genomic medicine. 31084224 2019
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.070 GeneticVariation disease BEFREE Blau syndrome (BS) is an autosomal dominant autoinflammatory disease associated with NOD2 gene mutations. 25381727 2017
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.070 GeneticVariation disease BEFREE Mutations in the nucleotide binding domain of the PRR, NOD2, are associated with the autoinflammatory diseases Blau syndrome and early-onset sarcoidosis. 28836875 2017
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.070 GeneticVariation disease BEFREE Dermatitis as a characteristic phenotype of a new autoinflammatory disease associated with NOD2 mutations. 23102769 2013
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.070 GeneticVariation disease BEFREE A new category of autoinflammatory disease associated with NOD2 gene mutations. 21914217 2011
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.070 GeneticVariation disease BEFREE Mutations in Nod2 have been associated with autoinflammatory disease in humans, including Crohn's disease. 17057187 2006
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.070 Biomarker disease BEFREE Sequence variations in the gene products PYPAF1/CIAS1 and NOD2/CARD15 have been associated with several autoinflammatory diseases that, although clinically different, share a similar inflammatory pathophysiology. 14630645 2003