Disease: Choroidal Neovascularization ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0600518
Disease: Choroidal Neovascularization
Choroidal Neovascularization 		0.020 Biomarker phenotype LHGDN We genotyped three SNPs, rs1061170 (exon 9, CFH), rs11200638 (HTRA1 promoter, -512 bp), and rs10490924 (6.6 kb upstream of HTRA1 in LOC387715/ARMS2) in 333 cases with advanced AMD (choroidal neovascularization [CNV] and geographic atrophy) and 171 age-matched examined controls. 18682806 2008
CUI: C0600518
Disease: Choroidal Neovascularization
Choroidal Neovascularization 		0.020 GeneticVariation phenotype LHGDN Myopic choroidal neovascularization genetics. 18762075 2008