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DDIEM: drug database for inborn errors of metabolism.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Abdelhakim, Marwa 
McMurray, Eunice 
Syed, Ali Raza 
Kafkas, Senay 
Kamau, Allan Anthony 

Abstract

BACKGROUND: Inborn errors of metabolism (IEM) represent a subclass of rare inherited diseases caused by a wide range of defects in metabolic enzymes or their regulation. Of over a thousand characterized IEMs, only about half are understood at the molecular level, and overall the development of treatment and management strategies has proved challenging. An overview of the changing landscape of therapeutic approaches is helpful in assessing strategic patterns in the approach to therapy, but the information is scattered throughout the literature and public data resources. RESULTS: We gathered data on therapeutic strategies for 300 diseases into the Drug Database for Inborn Errors of Metabolism (DDIEM). Therapeutic approaches, including both successful and ineffective treatments, were manually classified by their mechanisms of action using a new ontology. CONCLUSIONS: We present a manually curated, ontologically formalized knowledgebase of drugs, therapeutic procedures, and mitigated phenotypes. DDIEM is freely available through a web interface and for download at http://ddiem.phenomebrowser.net.

Description

Keywords

Drug effect, Drug repositioning, Inborn errors of metabolism, Ontology, Orphan disease, Therapeutic procedure, Databases, Pharmaceutical, Humans, Metabolism, Inborn Errors, Phenotype, Rare Diseases

Journal Title

Orphanet J Rare Dis

Conference Name

Journal ISSN

1750-1172
1750-1172

Volume Title

15

Publisher

Springer Science and Business Media LLC