The association between KCNH5 (Potassium Voltage-Gated Channel Subfamily H Member 5) and Developmental And Epileptic Encephalopathy 112 is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.
Sources3
Clinical variants8
Symptoms36
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.