Gard zidarie pret Rare diseases found on GARD should not be used as policy statements of NCATS or the NIH. The mission of the Genetic and Rare Diseases (GARD) Information Center is to help the rare disease community meet these common challenges. The mission of the Genetic and Rare Diseases (GARD) Information Center is to help the rare disease community meet these common challenges. These resources address common needs of rare disease patients and families, including contact information for rare disease centers outside of the United States. Filter by category or search by disease name, acronym, or synonym. Learn about the Genetic and Rare Diseases Information Center, the GARD website and its policies, and how to access data used on the GARD website. GARD collects data from a variety of sources to populate its website and provide accurate and reliable information on rare diseases. Contact a GARD Information Specialist if you need help finding more information on this rare disease or available clinical studies. We do this by providing free access to reliable and easy-to-understand information. . Welcome to GARD’s Support Center Explore trusted tools and resources—all in one place. Please note that GARD cannot enroll individuals in clinical studies. Important: GARD provides information about genetic and rare diseases for your general knowledge and is not a substitute for medical advice. GARD uses data collected from Orphanet, Online Mendelian Inheritance in Man (OMIM) , and Mondo Disease Ontology to interpret and provide information on rare diseases. Browse by Disease Explore GARD's list of rare diseases. Whether you're looking for medical specialists, patient support groups, or reliable health information, we're here to help you find what you need.