Hypertrophic cardiomyopathy 1

Definition

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

Also known as 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, CMH1, hypertrophic cardiomyopathy 1, hypertrophic cardiomyopathy caused by mutation in MYH7, hypertrophic cardiomyopathy type 1, MYH7 hypertrophic cardiomyopathy — per MONDO

Also identified as

• DOID 0110307 per MONDO
• OMIM 192600 per MONDO
• UMLS C3495498 per MONDO