Search for "Rare diseases" in article titles:

1. Rare Diseases Act of 2002: The Rare Disease Act of 2002 is a law passed in the United States that establishes the statutory authorization for the Office of Rare Diseases as a federal entity able to recommend a national research agenda, coordinate research, and provide ... (US law) [100%] 2023-08-16 [National Institutes of Health] [Rare diseases]...
2. ICD coding for rare diseases: The ICD coding for rare diseases is the International Classification of Diseases code used for the purpose of documenting rare diseases. It is important for health insurance reimbursement, administration, epidemiology, and research. (Medicine) [100%] 2023-10-11 [Clinical procedure classification] [Rare diseases]...
3. Office of Rare Diseases Research: The Office of Rare Diseases Research is a division of the National Center for Advancing Translational Sciences (NCATS) that oversees the Rare Diseases Clinical Research Network and Genetic and Rare Diseases Information Center. The Office of Rare Diseases Research was ... (Organization) [100%] 2023-07-18 [National Institutes of Health]
4. Rare Diseases Clinical Research Network: The Rare Diseases Clinical Research Network (RDCRN) is an initiative of the Office of Rare Diseases Research (ORDR). RDCRN is funded by the ORDR, the National Center for Advancing Translational Sciences and collaborating institute centers. (Medicine) [100%] 2023-07-30 [National Institutes of Health] [Rare diseases]...
5. European Organisation for Rare Diseases: The European Organisation for Rare Diseases (EURORDIS) is a non-governmental patient-driven alliance of patient organizations and individuals active in the field of rare diseases, that promotes research on rare diseases and commercial development of orphan drugs. EURORDIS is ... (Organization) [100%] 2023-09-23 [Biobank organizations]
6. Rare Diseases Clinical Research Network: The Rare Diseases Clinical Research Network (RDCRN) is funded by the National Institutes of Health (NIH) and led by the National Center for Advancing Translational Sciences (NCATS) through its Division of Rare Diseases Research Innovation (DRDRI). The RDCRN is designed ... [100%] 2025-03-19 [National Institutes of Health] [Rare disease organizations]...
7. Center of expertise for rare diseases: A Center of expertise for rare diseases is a physical expert structure for the management and care of rare disease patients. In the United Kingdom the more commonly used term is "centre of excellence". (Medicine) [91%] 2024-01-06 [Rare diseases]
8. Rare Diseases Clinical Research Network Contact Registry: The Rare Diseases Clinical Research Network (RDCRN) Contact Registry is a patient contact registry sponsored by the National Institutes of Health (NIH). The RDCRN Contact Registry collects and stores the contact information of people who want to participate in RDCRN ... (Medicine) [84%] 2023-12-05 [National Institutes of Health] [Rare diseases]...