作者
Ana Rath, Annie Olry, Ferdinand Dhombres, Maja Miličić Brandt, Bruno Urbero, Segolene Ayme
发表日期
2012/5
期刊
Human mutation
卷号
33
期号
5
页码范围
803-808
出版商
Wiley Subscription Services, Inc., A Wiley Company
简介
Rare disorders are scarcely represented in international classifications and therefore invisible in information systems. One of the major needs in health information systems and for research is to share and/or to integrate data coming from heterogeneous sources with diverse reference terminologies. ORPHANET (www.orpha.net) is a multilingual information portal on rare diseases and orphan drugs. Orphanet information system is supported by a relational database built around the concept of rare disorders. Representation of rare diseases in Orphanet encompasses levels of increasing complexity: lexical (multilingual terminology), nosological (multihierarchical classifications), relational (annotations—epidemiological data—and classes of objects—genes, manifestations, and orphan drugs—integrated in a relational database), and interoperational (semantic interoperability). Rare disorders are mapped to …
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