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Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CALR3 gene.
No clinical trials have been registered for hypertrophic cardiomyopathy 19.
2 publications have been identified in PubMed for hypertrophic cardiomyopathy 19. Kisho has analyzed 1 by research type. Research spans Epidemiology / Natural History (100%).
Sayed A (2025). [PMID: 40133243](https://pubmed.ncbi.nlm.nih.gov/40133243/). *J Am Heart Assoc*. [Epidemiology / Natural History]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 1:47 AM UTC
Online Mendelian Inheritance in Man