Cardiomyopathy, familial restrictive, 3

Definition

Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.

Also known as cardiomyopathy, familial restrictive, 3, cardiomyopathy, familial restrictive, type 3, familial isolated restrictive cardiomyopathy caused by mutation in TNNT2, TNNT2 familial isolated restrictive cardiomyopathy — per MONDO

Also identified as

• DOID 0111427 per MONDO
• MESH C567316 per MONDO
• OMIM 612422 per MONDO
• UMLS C2676271 per MONDO