Additional Resources

Section

NORD rare disease drug development ad.

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

Interested in exploring the database in detail?
Click here to explore the database in alphabetical order.

hypertrophic cardiomyopathy 4

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.

Print

Disease Overview

An autosomal dominant condition caused by mutation(s) in the MYBPC3 gene, encoding MYBPC3 protein. It is characterized by severe neonatal hypertrophic cardiomyopathy.

Synonyms

  • CMH4
  • MYBPC3 hypertrophic cardiomyopathy
  • cardiomyopathy, familial hypertrophic, 4
  • cardiomyopathy, familial hypertrophic, 4, susceptibility to
  • cardiomyopathy, familial hypertrophic, type 4
  • cardiomyopathy, hypertrophic, 4
  • familial hypertrophic cardiomyopathy type 4
  • hypertrophic cardiomyopathy 4
  • hypertrophic cardiomyopathy caused by mutation in MYBPC3
  • hypertrophic cardiomyopathy type 4
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.

View report
Sign Up for NORD News