LOXL1, lysyl oxidase like 1, 4016

N. diseases: 93; N. variants: 27
Disease: Venous retinal branch occlusion ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339505
Disease: Venous retinal branch occlusion
Venous retinal branch occlusion 		0.010 GeneticVariation disease BEFREE The results suggested that LOXL1 variants, well established markers for EX, are not likely genetic markers for BRVO in Japanese subjects. 22194657 2011