Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Disorder of macula of retina
CUI: C0730362
Disease: Disorder of macula of retina
0.010 GeneticVariation BEFREE It was noted that SRNVM is a rare occurrence in R345W fibulin-3 maculopathy. 16799055 2006