The association between OVOL2 (Ovo Like Zinc Finger 2) and Corneal Dystrophy, Posterior Polymorphous, 1 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.
Sources4
Clinical variants7
Symptoms50
Compounds0
Trials0
Publications4
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.