The association between SLC25A13 (Solute Carrier Family 25 Member 13) and Citrullinemia Type Ii 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 variants85
Symptoms47
Compounds0
Trials0
Publications33
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.