The association between SLC25A3 (Solute Carrier Family 25 Member 3) and Cardiomyopathy-Hypotonia-Lactic Acidosis Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources3
Clinical variants40
Symptoms11
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.