The association between TRMT10C (TRNA Methyltransferase 10C, Mitochondrial RNase P Subunit) and Combined Oxidative Phosphorylation Deficiency 30 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants4
Symptoms36
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.