The association between COL18A1 (Collagen Type XVIII Alpha 1 Chain) and Knobloch Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources3
Clinical variants258
Symptoms30
Compounds0
Trials0
Publications18
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.