Hypertrophic cardiomyopathy 10

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene.

Also known as cardiomyopathy, familial hypertrophic, 10, cardiomyopathy, familial hypertrophic, type 10, cardiomyopathy, hypertrophic, 10, CMH10, hypertrophic cardiomyopathy 10, hypertrophic cardiomyopathy caused by mutation in MYL2, hypertrophic cardiomyopathy type 10, MYL2 hypertrophic cardiomyopathy — per MONDO

Also identified as

• DOID 0110316 per MONDO
• MESH C563865 per MONDO
• OMIM 608758 per MONDO
• UMLS C1834460 per MONDO