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Latest : 1099 (2013-01-30)
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Welcome to the web pages of RAMEDIS, the Rare Metabolic Diseases Database.
The RAMEDIS system is a platform independent, web-based information system for rare metabolic diseases based on filed case reports. It was developed in close cooperation with clinical partners to allow them to collect information on rare metabolic diseases with extensive details, e.g. about occurring symptoms, laboratory findings, therapy and molecular data. By using largely standardized medical terms and conditions, the contents of the database are easy to compare and to analyze. In addition, a convenient graphical user interface is provided to the user accessible by every common web browser. RAMEDIS supports an extensible number of different genetic diseases and enables co-operative studies.
To be most effective, RAMEDIS employs help of medical doctors, biochemists, scientists who want to publish their case studies electronically in a rapid and comfortable way. Thus far, 818 patients have been published with 93 different genetic metabolic diseases. As a universal resource, RAMEDIS allows researchers to extract a diversity of standardized data types, including clinical, biochemical, and molecular. We expect RAMEDIS to continue to grow with your help, providing increasing amounts of knowledge to future generations. To access the case reports of RAMEDIS, please use Search/Browse.
This database despite being open to public access, is subject to copyright. Any use of data contained within this web site must receive appropriate acknowledgement and credit, meaning you should contact the author of the published data and cite the URL (http://www.ramedis.de).
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