Dilated cardiomyopathy 1X

Definition

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the FKTN gene.

Also known as cardiomyopathy, dilated, type 1X, CMD1X, dilated cardiomyopathy type 1X, familial isolated dilated cardiomyopathy caused by mutation in FKTN, FKTN familial isolated dilated cardiomyopathy — per MONDO

Also identified as

• DOID 0110444 per MONDO
• MESH C566907 per MONDO
• OMIM 611615 per MONDO
• UMLS C1969024 per MONDO