The association between SDCCAG8 (SHH Signaling And Ciliogenesis Regulator SDCCAG8) and Bardet-Biedl Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic and likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants15
Symptoms97
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.