hypertrophic cardiomyopathy 1 (MONDO_0008647) is any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene. Also known as: CMH1, MYH7 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic 1, cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant, cardiomyopathy, familial hypertrophic, type 1, cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant, cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant, hypertrophic cardiomyopathy caused by mutation in MYH7.