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IEMbase is a tool to help physicians in the interpretation of clinical and biochemical data of inborn errors of metabolism (IEMs).

In addition to using this app and before making any medical decisions, the users should seek a doctor’s advice.

There are currently 1,596 disorder entries, 3,679 biochemical or clinical phenotype entries, and 9,679 disorder-phenotype association entries in the database.

IEMbase features: Easy browsing through IEMs; Simple search for any IEM or term; Mini-expert system to search for a combination of clinical symptoms and biochemical markers and their deviations; Biochemical tests panel; Gene panel; Age-related clinical symptoms; Age-related biochemical markers; Disease and Gene information.

The editors and authors of IEMbase have made every effort to ensure that all information in this database is in accordance with the state of knowledge at the time of production. Nevertheless, the authors and editors are not responsible for errors or omissions or for the specific content of the database. Especially, we cannot guarantee the accuracy of data contained in this database. Every user should carefully examine the patient and laboratory data and should carefully check whether the information differ from statements made in the database.

Medical Disclaimer
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