CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Atrophic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0333641
Disease: Atrophic
Atrophic 		0.020 Biomarker phenotype LHGDN Joint effects of polymorphisms in the HTRA1, LOC387715/ARMS2, and CFH genes on AMD in a Caucasian population. 18682806 2008
CUI: C0333641
Disease: Atrophic
Atrophic 		0.020 GeneticVariation phenotype LHGDN Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokers. 16431947 2006