Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8929
Gene Symbol: PHOX2B
PHOX2B
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.330 GeneticVariation BEFREE IL23R, NOD2/CARD15, ATG16L1 and PHOX2B polymorphisms in a group of patients with Crohn's disease and correlation with sub-phenotypes. 21206965

2011
Entrez Id: 8929
Gene Symbol: PHOX2B
PHOX2B
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.330 GeneticVariation BEFREE In contrast, all analyzed SNPs in NOD2/CARD15, IL23R, and ATG16L1 were strongly associated with CD with P values ranging from 5.0x10(-3) to 1.6x10(-22), but there was no epistasis with polymorphisms in PHOX2B, NCF4, FAM92B, and rs224136. 19262523

2009
Entrez Id: 8929
Gene Symbol: PHOX2B
PHOX2B
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.330 Biomarker BEFREE Genome-wide association studies have identified PHOX2B, FAM92B, IRGM and NCF4 as candidate susceptibility factors for ileal Crohn's disease (CD). 18580884

2008
Entrez Id: 8929
Gene Symbol: PHOX2B
PHOX2B
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.330 Biomarker CTD_human Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007