The association between SLC16A1 (Solute Carrier Family 16 Member 1) and Ketoacidosis Due To Monocarboxylate Transporter-1 Deficiency is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic and likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants12
Symptoms0
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.