The association between SLC5A5 (Solute Carrier Family 5 Member 5) and Thyroid Dyshormonogenesis 1 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.
Sources4
Clinical variants117
Symptoms19
Compounds0
Trials0
Publications18
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.