The association between CCDC22 (CCC Complex Scaffolding Subunit CCDC22) and Ritscher-Schinzel Syndrome 1 is a manually-curated gene–disease association, drawing on a single expert-curated source, which records a causative germline mutation.
Sources1
Clinical variants2
Symptoms87
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.