NOTCH4, notch receptor 4, 4855

N. diseases: 150; N. variants: 58
Disease: Systemic Scleroderma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.120 GeneticVariation disease BEFREE These results suggest that modulation of the NOTCH4 gene might be responsible for the association signal at chromosome 6p21 in SSc. 27829420 2016
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.120 GeneticVariation disease GWASCAT Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. 21779181 2011
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.120 GeneticVariation disease GWASDB Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. 21779181 2011
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.120 GeneticVariation disease BEFREE Within the HLA region, HLA-DQB1, HLA-DPA1/B1, and NOTCH4 associations with SSc are likely confined to specific auto-antibodies. 21779181 2011
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.120 GeneticVariation disease GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147 2010