Cardiomyopathy, familial restrictive, 1

Definition

Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene.

Also known as cardiomyopathy, familial restrictive, 1, cardiomyopathy, familial restrictive, type 1, familial isolated restrictive cardiomyopathy caused by mutation in TNNI3, TNNI3 familial isolated restrictive cardiomyopathy — per MONDO

Also identified as

• DOID 0111425 per MONDO
• MESH C566168 per MONDO
• OMIM 115210 per MONDO
• UMLS C1861861 per MONDO