The association between EPS8L2 (EPS8 Signaling Adaptor L2) and Deafness, Autosomal Recessive 106 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic and likely-pathogenic variants.
Sources3
Clinical variants20
Symptoms2
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.