Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.500 GeneticVariation LHGDN Role of CARD15, DLG5 and OCTN genes polymorphisms in children with inflammatory bowel diseases. 17451203

2007

Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.500 GeneticVariation LHGDN Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD). 16333318

2006

Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.500 GeneticVariation LHGDN Phenotype-genotype associations were evaluated in a Canadian cohort including 507 patients with CD, 216 patients with UC, and 352 ethnically matched controls genotyped for SLC22A4 C1672T, SLC22A5 G-207C, and the major CD-associated CARD15 variants. 15685536

2005

Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.500 GeneticVariation LHGDN Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease. 16437728

2005

Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.500 GeneticVariation LHGDN These results suggest that SLC22A4, SLC22A5 and CARD15 act in a common pathogenic pathway to cause Crohn disease. 15107849

2004