Hypertrophic cardiomyopathy 17

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the JPH2 gene.

Also known as cardiomyopathy, familial hypertrophic, type 17, cardiomyopathy, hypertrophic, 17, CMH17, hypertrophic cardiomyopathy caused by mutation in JPH2, hypertrophic cardiomyopathy type 17, JPH2 hypertrophic cardiomyopathy — per MONDO

Also identified as

• DOID 0110323 per MONDO
• OMIM 613873 per MONDO
• UMLS C3151264 per MONDO