The association between AKT1 (AKT Serine/Threonine Kinase 1) and Cowden Syndrome 6 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources4
Clinical variants486
Symptoms11
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.