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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 | 841 |
| cell types | Cell Ontology | 186 |
| chemicals | CHEBI | 378 |
| disease drivers | Disease Drivers Ontology | 19 |
| evidence codes | Evidence and Conclusion Ontology | 13 |
| food material | FoodOn Ontology | 59 |
| inheritance pattern | Genotype Ontology | 29 |
| omim susceptibility (genetic risk factors) | OMIM susceptibility terms | 201 |
| ontology relations | Relations Ontology | 41 |
| onset | Human Phenotype Ontology | 14 |
| phenotypes | Human Phenotype Ontology | 527 |
| sequence structural and functional variants | Sequence Ontology | 252 |
| symptoms | Symptom Ontology | 894 |
| taxonomy | NCBI Taxonomy | 1,172 |
| transmission methods | Pathogen Transmission Ontology | 32 |
