The association between TBC1D32 (TBC1 Domain Family Member 32) and Orofaciodigital Syndrome Ix is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and a causative germline mutation.
Sources3
Clinical variants2
Symptoms90
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.