The association between RAG1 (Recombination Activating 1) 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 variants, and a causative germline mutation.
Sources5
Clinical variants190
Symptoms110
Compounds0
Trials0
Publications31
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.