The association between DCLRE1C (DNA Cross-Link Repair 1C) and Omenn Syndrome is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants217
Symptoms110
Compounds0
Trials0
Publications5
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.