The association between SCNM1 (Sodium Channel Modifier 1) and Orofaciodigital Syndrome Xix is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources3
Clinical variants3
Symptoms66
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.