The association between LCA5 (Lebercilin LCA5) and Leber Plus Disease is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants54
Symptoms29
Compounds0
Trials0
Publications8
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.