Hypertrophic cardiomyopathy 8

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene.

Also known as cardiomyopathy, familial hypertrophic, 8, cardiomyopathy, familial hypertrophic, type 8, cardiomyopathy, hypertrophic, 8, hypertrophic cardiomyopathy 8, hypertrophic cardiomyopathy caused by mutation in MYL3, hypertrophic cardiomyopathy type 8, MYL3 hypertrophic cardiomyopathy — per MONDO

Also identified as

• DOID 0110314 per MONDO
• MESH C563866 per MONDO
• OMIM 608751 per MONDO
• UMLS C1837471 per MONDO