RDCRN

A rare disease is defined by the U.S. National Institutes of Health Office of Rare Diseases as one that affects fewer than 200,000 people in the United States. The Rare Diseases Clinical Research Network (RDCRN) is designed to advance medical research on rare diseases by providing support for clinical studies and facilitating collaboration, study enrollment and data sharing. Through the RDCRN consortia, physician scientists and their multidisciplinary teams work together with patient advocacy groups to study more than 200 rare diseases at sites across the nation.

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