The association between SLC25A11 (Solute Carrier Family 25 Member 11) and Pheochromocytoma/Paraganglioma Syndrome 6 is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources3
Clinical variants7
Symptoms5
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.