#What Do I Know About Rare Diseases ?

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What is Orphanet?

Orphanet is an information portal on rare diseases, created in 1996 jointly by INSERM and the DGS, first in French and then translated into six other languages to become the global reference portal.

Orphanet is a unique resource, gathering and improving knowledge on rare diseases, in order to facilitate and improve the diagnosis, care and treatment of patients with rare diseases. Orphanet’s objective is to provide high quality information on rare diseases and to allow the same access to knowledge for all stakeholders (researchers, patients, caregivers…). Orphanet is also developing Orphanet’s nomenclature on rare diseases (ORPHA code), which is essential for improving the visibility of rare diseases in health and research information systems.

For more information go to => https://www.orpha.net/consor/cgi-bin/index.php?lng=FR