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- Genetic and Rare Diseases Information Center | GARD
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
- Diseases | GARD
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 phone 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
GARD collects data from a variety of sources to populate its website and provide accurate and reliable information on rare diseases GARD uses data collected from Orphanet, Online Mendelian Inheritance in Man (OMIM) , and Mondo Disease Ontology to interpret and provide information on rare diseases This includes names, synonyms, genes, symptom
- Myofibrillar myopathy | About the Disease | GARD - Genetic and Rare . . .
GARD uses data collected from Orphanet, Online Mendelian Inheritance in Man (OMIM) , and Mondo Disease Ontology to interpret and provide information on rare diseases This includes names, synonyms, genes, symptom frequency, population estimates and more
- Centro de Información sobre Enfermedades Raras y Genéticas | GARD
GARD brinda acceso a información y recursos actuales, confiables y claros Utilizar el respaldo que GARD ofrece puede contribuir a asegurar que reciba la mejor atención posible para su enfermedad rara
- Campomelic dysplasia | About the Disease | GARD - Genetic and Rare . . .
GARD uses data collected from Orphanet, Online Mendelian Inheritance in Man (OMIM) , and Mondo Disease Ontology to interpret and provide information on rare diseases This includes names, synonyms, genes, symptom frequency, population estimates and more
- Chromosome 1p36 deletion syndrome | About the Disease | GARD
Currently, GARD aims to provide the following information for this disease: Population Estimate: Fewer than 200,000 people in the U S have this disease Symptoms: May start to appear during Pregnancy and as a Newborn
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