Genetic and Rare Diseases Information Center | GARD GARD provides access to information and resources that are current, reliable, and clear Using the support GARD offers can help ensure you are getting the best possible care for your rare disease Here, learn what kind of information and resources GARD offers
Diseases | GARD 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
Contact Us | GARD - Genetic and Rare Diseases Information Center We invite patients, family members, caregivers, and others seeking information about rare diseases to contact GARD by leaving us a detailed voice message or through our contact form Our Information Specialists provide personalized responses that are easy to understand, free of charge, and confidential
About | GARD - Genetic and Rare Diseases Information Center What should you know 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
Centro de Información sobre Enfermedades Raras y Genéticas | GARD Comuníquese con GARD Los Especialistas en Información de GARD brindan ayuda individualizada para conectarle con información y recursos Nuestros Especialistas en Información pueden ayudarle: Encontrar o comprender información sobre una enfermedad rara Navegar por la información sobre cómo obtener un diagnóstico de una enfermedad rara
Enfermedades | GARD - Genetic and Rare Diseases Information Center Enfermedades Enfermedades Explore la lista de enfermedades raras de GARD Puede filtrar por categoría o buscar por nombre de la enfermedad, acrónimo o sinónimo Las enfermedades raras encontradas en GARD no deben utilizarse como declaraciones políticas del NCATS o de los NIH Por favor, tenga en cuenta que los nombres de las enfermedades sólo están disponibles en inglés
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What should you know 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
Hereditary spherocytosis | About the Disease | GARD Hereditary spherocytosis is a condition characterized by hemolytic anemia (when red blood cells are destroyed earlier than normal) Symptoms can range from mild to severe and may include pale skin, fatigue, anemia, jaundice, gallstones, and or enlargement of the spleen Other symptoms of hemolytic anemia may include feeling that your heart is pounding or racing (palpitations), feeling dizzy
Hypophosphatasia | About the Disease | GARD Please note: GARD provides organizations for informational purposes only and not as an endorsement of their services Contact a GARD Information Specialist for more information on organizations that may be dedicated to this disease Please contact an organization directly if you have questions about the information or resources it provides