Disease Ontology

Known as: DOID, Disease Ontology Identifier, Human Disease Ontology 
The Disease Ontology (DO) is a formal ontology of human disease. The Disease Ontology project is hosted at the Institute for Genome Sciences at the… (More)
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Highly Cited
2015
Highly Cited
2015
The current version of the Human Disease Ontology (DO) (http://www.disease-ontology.org) database expands the utility of the… (More)
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2013
2013
BACKGROUND We are developing the Neurological Disease Ontology (ND) to provide a framework to enable representation of aspects of… (More)
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Highly Cited
2012
Highly Cited
2012
The Disease Ontology (DO) database (http://disease-ontology.org) represents a comprehensive knowledge base of 8043 inherited… (More)
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Review
2011
Review
2011
Fragile X syndrome (FXS) is the most common inherited form of mental retardation and a leading known cause of autism. It is… (More)
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Highly Cited
2009
Highly Cited
2009
Subjective methods have been reported to adapt a general-purpose ontology for a specific application. For example, Gene Ontology… (More)
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Review
2006
Review
2006
Airway inflammation is central to the pathogenesis of both airway remodelling and parenchymal destruction in chronic obstructive… (More)
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2005
2005
In this paper, we discuss an ontology-based system and approach that provides interoperability support for research in, and… (More)
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Highly Cited
2000
Highly Cited
2000
Multi-level research that attempts to describe ecological effects in themselves (for example, the effect on individual health… (More)
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Highly Cited
1991
Highly Cited
1991
THE human prion diseases, Creutzfeldt–Jakob disease (CJD) and Gerstmann–Sträussler syndrome (GSS), are neurodegenerative diseases… (More)
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Highly Cited
1984
Highly Cited
1984
A prospective study was initiated in January 1980 to follow with Duplex scanning a consecutive series of 167 asymptomatic… (More)
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