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- List of Rare Diseases | A-Z Database | NORD
What Is the NORD ® Rare Disease Database? The NORD Rare Disease Database is an inclusive and comprehensive list of rare diseases based on information from established rare disease ontologies and it is an ongoing project made possible by a close collaboration with MONDO, Orphanet, and Online Mendelian Inheritance in Man (OMIM) The NORD Rare Disease Database includes: NORD Rare Disease Reports
- National Organization for Rare Disorders | NORD
We provide information about rare diseases, patient organizations and other resources We also promote awareness of rare diseases among physicians and other medical professionals
- Rare Disease Facts and Statistics | NORD
Rare Disease at a Glance 1 in 10 Americans live with a rare disease, half of whom are children Of more than 10,000 known rare diseases, fewer than 5% have an approved treatment People living with rare disease face medical costs that are 3-5 times higher than people with non-rare conditions
- Rare Disease News - National Organization for Rare Disorders
Stay informed with the latest rare disease research, breakthrough treatments, and patient stories from NORD's expert team of medical professionals
- Centers of Excellence - National Organization for Rare Disorders
In addition, researchers at each Rare Disease Center of Excellence are working with doctors and patients to find more treatments and cures for rare diseases NORD is interconnecting this Network of major academic medical and research institutions to encourage collaboration and sharing of best practices and expertise
- Rare Diseases Support, Resources Help | NORD
Can NORD help find a medical expert for my rare disease? Many patient organizations provide lists of medical experts Search NORD’s Organizational Database to find disease-specific patient advocacy organizations NORD Rare Disease Centers of Excellence are diagnosing and treating thousands of rare disease patients
- Rare Disease UK - National Organization for Rare Disorders
The Rare Disease UK is the non-profit, National Alliance for rare diseases and all who support them in the United Kingdom Their members include patient organizations, researchers, academics, clinicians, individuals and pharmaceutical companies
- Patient Organizations - National Organization for Rare Disorders
Understanding Rare Disease Where to start Rare Disease Facts and Statistics NORD’s Rare Disease Database Rare Disease Video Library Help for People with Undiagnosed Medical Conditions Find A Rare Disease Organization
- Duke Health Rare Disease Center
Undiagnosed Diseases Network (UDN) Clinical Site The UDN is a research study funded by the National Institutes of Health There are currently 24 clinical sites, including Duke University Participants in the UDN are determined by a central application process Serves both children and adults
- Rare Disease Research - National Organization for Rare Disorders
Accelerate rare disease research through strategic funding, collaborative partnerships, and innovative approaches to understanding complex medical conditions
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