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Diseases

Genetic and Rare Diseases Information Center (GARD)

Familial dilated cardiomyopathy


Other Names for this Disease
  • Dilated cardiomyopathy, familial
  • Cardiomyopathy, familial dilated
  • Hypokinetic dilated cardiomyopathy, familial
  • Familial isolated dilated cardiomyopathy
  • Familial or idiopathic dilated cardiomyopathy
Related Diseases
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

News & Events


ORDR Co-Sponsored Conferences

  • 2016 Rare Disease Day at NIH, Monday, February 29, 2016
    Location: Building 10, Masur Auditorium, National Institutes of Health, Bethesda, MD
    Description: The 2016 Rare Disease Day at NIH will take place on February 29. The event, sponsored by NCATS and the NIH Clinical Center, aims to raise awareness about rare diseases, the patients they affect and the research collaborations that are addressing rare disease challenges. The day will feature tours, posters and exhibits, and presentations.

  • The 11th Annual North American Genetic Analysis of ABC Transporters Workshop, Wednesday, September 24, 2014 - Thursday, September 25, 2014
    Location: NCI-Frederick, Frederick, MD
    Description: <p>This workshop features presentations from graduate students, post-docs., and senior investigators studying the role of ATP Cassette Binding Proteins in human disease. Phylogenetic studies, model systems, and bioinformatic techniques that shed light in this rapidly developing research area are presented. Because student presentations predominate, unpublished results often are first disclosed at these workshops.</p>

  • Gordon Research Conference – Intermediate Filaments, Saturday, June 14, 2014 - Friday, June 20, 2014
    Location: Mount Snow Resort, West Dover, VT
    Description: <p>The 2014 GRC-Intermediate Filaments will include short talks, discussions, and poster presentations from the leaders in the field. It will provides several functional perspectives with an emphasis on the paradigm shifting notion that IFs are not only structural proteins but also play essential roles as signaling organizers and buffers of cellular stress, which contribute to number of disease pathologies. There will be robust discussions on how mutations in the IF genes encoding these IF proteins are responsible for rare diseases, such as epidermolysis bullosa simplex (EBS), but extending into the entire list of rare diseases outlined above.<span>&nbsp; </span>Discussions will be focused on how cell biology and physiology efforts are providing unique therapeutic approaches to the highly complex disorders, such as those caused by lamin A/C gene mutations, which are involved in Progeria.</p>

  • Fifth International Conference on Pediatric Mechanical Circulatory Support Systems and Pediatric Cardiopulmonary Perfusion , Thursday, May 28, 2009 - Saturday, May 30, 2009
    Location: Hilton Anatole, Dallas, TX
    Description: The main objective of this conference was to focus on the current problems associated with pediatric cardiac patients during and after acute or chronic cardiac support. At this conference, we brought together many distinguished physicians and scientists to define precisely the current problems and to suggest solutions with novel approaches.

Other Names for this Disease
  • Dilated cardiomyopathy, familial
  • Cardiomyopathy, familial dilated
  • Hypokinetic dilated cardiomyopathy, familial
  • Familial isolated dilated cardiomyopathy
  • Familial or idiopathic dilated cardiomyopathy
Related Diseases
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.