The association between TBC1D8B (TBC1 Domain Family Member 8B) and Nephrotic Syndrome, Type 20 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.
Sources4
Clinical variants22
Symptoms10
Compounds0
Trials0
Publications5
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.