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The mission of the Genetic and Rare Diseases (GARD) Information Center is to help the rare disease community meet these common challenges. We do this by providing free access to reliable and easy-to-understand information.
Gard is a leading provider of marine insurance products and services, with a global network of offices and correspondents. Learn about Gard's history, news, insights, sustainability, and career opportunities.
Navigating a rare disease can be daunting. NIH's Genetic and Rare Diseases (GARD) Information Center offers reliable, easy-to-understand information in English and Spanish on thousands of rare diseases.
Browse by Disease Explore GARD's list of rare diseases. Filter by category or search by disease name, acronym, or synonym. Rare diseases found on GARD should not be used as policy statements of NCATS or the NIH.
We invite patients, family members, caregivers, and others seeking information about rare diseases to contact GARD by phone or through our contact form. Our Information Specialists provide personalized responses that are easy to understand, free of charge, and confidential.
About GARD GARD is a program of the National Institutes of Health that provides free access to reliable, easy-to-understand information about genetic and rare diseases.
Gard is a department in Southern France, named after the river Gardon. It has a history of Roman settlement, a Mediterranean coastline, and a population of about 764,000.
GARD is a service that provides information about genetic and rare diseases to patients, families, health professionals, and researchers. Contact GARD by phone, form, e-mail, or mail for current and accurate information in English or Spanish.
GARD provides multiple resources for individuals with rare diseases. There is a searchable database that will give easy to understand information on more than 6,500 conditions.
GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish. GARD Information Specialists are available by phone, email and contact form to assist families, health professionals, researchers, teachers and students in providing information about rare diseases.