LOXL1, lysyl oxidase like 1, 4016

N. diseases: 93; N. variants: 27
Disease: Central retinal vein occlusion ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0154841
Disease: Central retinal vein occlusion
Central retinal vein occlusion 		0.010 GeneticVariation disease BEFREE The results suggested that the LOXL1 variants, which are well-established markers for EX, are not likely genetic markers for CRVO in Japanese subjects. 25130441 2015