The association between GPHN (Gephyrin) and Molybdenum Cofactor Deficiency, Type C is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants707
Symptoms35
Compounds0
Trials0
Publications9
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.