Hypertrophic cardiomyopathy 13

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNC1 gene.

Also known as cardiomyopathy, familial hypertrophic, type 13, cardiomyopathy, hypertrophic, 13, CMH13, hypertrophic cardiomyopathy caused by mutation in TNNC1, hypertrophic cardiomyopathy type 13, TNNC1 hypertrophic cardiomyopathy — per MONDO

Also identified as

• DOID 0110319 per MONDO
• MESH C567686 per MONDO
• OMIM 613243 per MONDO
• UMLS C2750472 per MONDO