The term hypertrophic cardiomyopathy (HCM) encompasses all myocardial diseases characterized by left ventricular hypertrophy that cannot be explained by pathological alterations in afterload or preload such as arterial hypertension or cardiac defects. Using the HCM register, important findings are obtained on the nature of the different HCM as well as on the ability to optimize diagnostic and treatment procedures and interventional procedures, for example with regard to predictors of and prophylaxis for arrhythmia, response rates to medication and interventional procedures (alcohol septal ablation, myectomy).