The association between KCNH2 (Potassium Voltage-Gated Channel Subfamily H Member 2) and Familial Hypertrophic Cardiomyopathy is supported by expert-curated evidence, drawing on a single expert-curated source, which records likely-pathogenic variants.
Sources1
Clinical variants1
Symptoms0
Compounds1
Trials0of 329 via KCNH2 compounds
Publications0
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.