GARD

GARD (Genetic and Rare Diseases Information Center) is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH). GARD provides the public with access to current, reliable, and easy-to-understand information about rare diseases and genetic disorders.

Overview[edit | edit source]

GARD was established to increase the availability of information about rare and genetic diseases, and to assist in the diagnosis and treatment of these conditions. The center provides information to health professionals, researchers, and the general public. It also serves as a resource for individuals and families who are dealing with rare or genetic diseases.

Services[edit | edit source]

GARD provides a variety of services to assist those seeking information about rare and genetic diseases. These include:

Disease Information: GARD maintains a database of detailed information on more than 6,000 rare and genetic diseases. This information includes symptoms, causes, treatment options, and resources for further information.

Information Specialists: GARD employs information specialists who can provide personalized responses to inquiries about specific diseases. These specialists can provide information in English or Spanish, and can assist with complex medical terminology.

Educational Resources: GARD provides a variety of educational resources, including fact sheets, brochures, and webinars. These resources are designed to help individuals understand rare and genetic diseases, and to assist health professionals in diagnosing and treating these conditions.

Contacting GARD[edit | edit source]

GARD can be contacted through their website, by phone, or by mail. The center's information specialists are available to answer questions and provide information on weekdays during regular business hours.