Discover how the Genetic and Rare Diseases Information Center Website and Contact Center can help patients and families who have a rare disease.
The Genetic and Rare Diseases (GARD) Information Center is a program of the National Center for Advancing Translational Sciences (NCATS) and is funded by the National Institutes of Health (NIH). GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English and Spanish. The website serves as a central point for information on rare diseases, offering resources for patients, families, healthcare providers, researchers, and the public.
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Comprehensive details on rare diseases, including symptoms, causes, and treatments.
Allows users to search for diseases by name, symptoms, or genetic cause.
Provides links to support groups, financial aid, and other resources for patients and families.
Offers tools and information for healthcare professionals to aid in diagnosis and treatment.
Includes details on clinical trials and research studies related to rare diseases.
Information available in multiple languages to cater to a diverse audience.
Regular updates on the latest research, treatments, and news related to rare diseases.
Option to contact GARD information specialists for personalized assistance.
National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).
Funded by the NIH, ensuring free access to all resources and information.
The website is designed to be accessible to all users, including those with disabilities.
Works with various organizations and experts worldwide to gather and disseminate accurate information.
Offers a range of educational materials for different audiences, including fact sheets and videos.
Security headers report is a very important part of user data protection. Learn more about http headers for rarediseases.info.nih.gov