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Diseases

Genetic and Rare Diseases Information Center (GARD)

Hereditary hemorrhagic telangiectasia type 2


Other Names for this Disease
  • HHT2
  • Osler Weber Rendu syndrome type 2
  • Telangiectasia hereditary hemorrhagic type 2
  • ORW2
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Research

On this page

Patient Registry

  • The Brain Vascular Malformation Consortium is a team of doctors, nurses, research coordinators, and research labs throughout the U.S., working together to improve the lives of people with familial cavernous malformations, Sturge-Weber syndrome, hereditary hemorrhagic telangiectasia through research. The Brain Vascular Malformation Consortium has a registry for patients who wish to be contacted about clinical research opportunities.

    For more information on the registry see: http://rarediseasesnetwork.epi.usf.edu/registry/index.htm
Other Names for this Disease
  • HHT2
  • Osler Weber Rendu syndrome type 2
  • Telangiectasia hereditary hemorrhagic type 2
  • ORW2
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.