Hypertrophic cardiomyopathy 20

Definition

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

Also known as cardiomyopathy, familial hypertrophic, type 20, cardiomyopathy, hypertrophic, 20, CMH20, hypertrophic cardiomyopathy caused by mutation in NEXN, hypertrophic cardiomyopathy type 20, NEXN hypertrophic cardiomyopathy — per MONDO

Also identified as

• DOID 0110326 per MONDO
• OMIM 613876 per MONDO
• UMLS C3151267 per MONDO