Orphanet is a unique resource, gathering and improving knowledge on rare diseases so as to improve the diagnosis, care and treatment of patients with rare ...
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Orphanet was established in France in 1997 at the advent of the internet in order to gather scarce knowledge on rare diseases.
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The ORPHANET is a database dedicated to providing information on rare diseases and orphan drugs. Its access is free of charge.
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Orphanet is an organisation and knowledge base dedicated to rare diseases as well as corresponding diagnosis, orphan drugs, clinical trials and expert ...
Orphanet uses the European definition of a rare disease, as defined by the European Union Regulation on Orphan Medicinal Products (1999), that being a disease ...
Rare diseases are diseases which affect a small number of people compared to the general population and specific issues are raised in relation to their rarity.
The Orphanet nomenclature is a multilingual, standardised, controlled medical terminology specific to rare diseases, that includes all clinical entities ...
A rare disorder for which all reasonable efforts have been done by rare diseases experts to determine a diagnosis according to the state of the art.
Sep 16, 2019 · Orphanet, as a European based resource, registers RDs with a point prevalence of <5 per 10 000, and diseases defined as rare in most ...
Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs.