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hypertrophic cardiomyopathy 1

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 MYH7 gene.

Synonyms

  • CMH1
  • Cmh
  • MYH7 hypertrophic cardiomyopathy
  • asymmetric septal Hypertrophy
  • cardiomyopathy, familial hypertrophic 1
  • cardiomyopathy, familial hypertrophic, 1
  • cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant
  • cardiomyopathy, familial hypertrophic, type 1
  • cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant
  • cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant
  • hypertrophic cardiomyopathy 1
  • hypertrophic cardiomyopathy caused by mutation in MYH7
  • hypertrophic cardiomyopathy type 1
  • hypertrophic subaortic stenosis, idiopathic
  • ventricular Hypertrophy, hereditary
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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