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Home > DO resources > DO Imports

DO Imports

The Human Disease Ontology integrates non-disease ontology terms to define connections between diseases, defined by logical axioms. Utilizing ontology imports enables exploration of disease terms through their related cell of origin, anatomical location, symptoms, phenotypes, genetic or environmental risk factors. DO import files are generated with each DO release using ROBOT extract, which syncs the import file with their source ontologies.

Data Type Source Terms
anatomy UBERON Ontology 792
cell types Cell Ontology 185
chemicals CHEBI 372
disease drivers Disease Drivers Ontology 19
evidence codes Evidence and Conclusion Ontology 13
food material FoodOn Ontology 58
inheritance pattern Genotype Ontology 29
omim susceptibility (genetic risk factors) OMIM susceptibility terms 202
ontology relations Relations Ontology 41
onset Human Phenotype Ontology 14
phenotypes Human Phenotype Ontology 429
sequence structural and functional variants Sequence Ontology 247
symptoms Symptom Ontology 889
taxonomy NCBI Taxonomy 1,137
transmission methods Transmission Process Ontology 32
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Last updated: Sep 2022
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