Hypertrophic cardiomyopathy 16

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene.

Also known as cardiomyopathy, familial hypertrophic, type 16, cardiomyopathy, hypertrophic, 16, CMH16, hypertrophic cardiomyopathy caused by mutation in MYOZ2, hypertrophic cardiomyopathy type 16, MYOZ2 hypertrophic cardiomyopathy — per MONDO

Also identified as

• DOID 0110322 per MONDO
• OMIM 613838 per MONDO
• UMLS C3151204 per MONDO