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hypertrophic cardiomyopathy 16

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene.

Synonyms

  • CMH16
  • MYOZ2 hypertrophic cardiomyopathy
  • cardiomyopathy familial hypertrophic 16
  • cardiomyopathy, familial hypertrophic, 16
  • cardiomyopathy, familial hypertrophic, type 16
  • cardiomyopathy, hypertrophic, 16
  • hypertrophic cardiomyopathy caused by mutation in MYOZ2
  • hypertrophic cardiomyopathy type 16
OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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