The association between SLC22A5 (Solute Carrier Family 22 Member 5) and Lipid Metabolism Disorder is reported, with clinical genetic testing available.
Sources1
Clinical variants0
Symptoms0
Compounds1
Trials22of 149 via SLC22A5 compounds
Publications0
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.