https://github.com/monarch-initiative/mondo/issues/4521

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene.

http://purl.obolibrary.org/obo/DOID_0110307, https://omim.org/entry/192600

cardiomyopathy, familial hypertrophic 1, cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant, cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant, cardiomyopathy, familial hypertrophic, type 1, hypertrophic cardiomyopathy caused by mutation in MYH7, hypertrophic cardiomyopathy type 1, hypertrophic cardiomyopathy 1, cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant, CMH1, MYH7 hypertrophic cardiomyopathy

cardiomyopathy, familial hypertrophic, 1, ventricular Hypertrophy, hereditary, asymmetric septal Hypertrophy, hypertrophic subaortic stenosis, idiopathic, Cmh

MONDO:0008647