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Mondo

This is the repository for managing the Mondo Disease Ontology (Mondo). Mondo aims to harmonizes disease definitions across the world. For more details on this ontology see:

Identifiers

Concepts in Mondo are represented by URIs like http://purl.obolibrary.org/obo/MONDO_0005015 or by compact URIs (CURIEs) with the prefix MONDO:, such as MONDO:0005015, as required by the OBO Foundry Identifier Policy.

Versions

Stable release versions

See Changes.md for more details

Editors' version

Editors of this ontology should use the edit version, src/ontology/mondo-edit.obo

Read the editors guide first!

https://mondo.readthedocs.io/en/latest/

Layout:

  • src/

Logo

The Mondo logo is available here: https://github.com/tis-lab/closed-illustrations/tree/master/logos/mondo-logos

Cite

Mondo: integrating disease terminology across communities, Nicole A Vasilevsky, Sabrina Toro, Nicolas Matentzoglu, Joseph E Flack, Kathleen R Mullen, Harshad Hegde, Sarah Gehrke, Patricia L Whetzel, Yousif Shwetar, Nomi L Harris, Mee S Ngu, Gioconda L Alyea, Megan S Kane, Paola Roncaglia, Eric Sid, Courtney L Thaxton, Valerie Wood, Roshini S Abraham, Maria Isabel Achatz, Pamela Ajuyah, Joanna S Amberger, Lawrence Babb, Jasmine Baker, James P Balhoff, Jonathan S Berg, Amol Bhalla, Xavier Bofill-De Ros, Ian R Braun, Eleanor C Broeren, Blake K Byer, Alicia B Byrne, Tiffany J Callahan, Leigh C Carmody, Lauren E Chan, Amanda R Clause, Julie S Cohen, Marcello DeLuca, Natalie T Deuitch, May Flowers, Jamie Fraser, Toyofumi Fujiwara, Vanessa Gitau, Jennifer L Goldstein, Dylan Gration, Tudor Groza, Benjamin M Gyori, William Hankey, Jason A Hilton, Daniel S Himmelstein, Stephanie S Hong, Charles T Hoyt, Robert Huether, Eric Hurwitz, Julius O B Jacobsen, Atsuo Kikuchi, Sebastian Köhler, Daniel R Korn, David Lagorce, Bryan J Laraway, Jane Y Li, Adriana J Malheiro, James McLaughlin, Birgit H M Meldal, Shruthi Mohan, Sierra A T Moxon, Monica C Munoz-Torres, Tristan H Nelson, Frank W Nicholas, David Ochoa, Daniel Olson, Tudor I Oprea, Tomiko T Oskotsky, David Osumi-Sutherland, Kelley Paris, Helen E Parkinson, Zoë M Pendlington, Xiao P Peng, Amy Pizzino, Sharon E Plon, Bradford C Powell, Julie C Ratliff, Heidi L Rehm, Lyubov Remennik, Erin R Riggs, Sean Roberts, Peter N Robinson, Justyne E Ross, Kevin Schaper, Brian M Schilder, Johanna L Schmidt, Elliott W Sharp, Morgan N Similuk, Damian Smedley, Tam P Sneddon, Rachel Sparks, Ray Stefancsik, Gregory S Stupp, Shilpa Sundar, Terue Takatsuki, Imke Tammen, Kezang C Tshering, Deepak R Unni, Eloise Valasek, Adeline Vanderver, Alex H Wagner, Ryan F Webb, Danielle Welter, Doron Yaya-Stupp, Andreas Zankl, Xingmin Aaron Zhang, Julie A McMurry, Christopher G Chute, Ada Hamosh, Christopher J Mungall, Melissa A Haendel, ClinGen DICER1 and miRNA-Processing Gene Variant Curation Expert Panel; ClinGen Hereditary Gene Curation Expert Panel; ClinGen Motile Ciliopathy Gene Curation Expert Panel; ClinGen Myeloid Malignancy Variant Curation Expert Panel; ClinGen TP53 Variant Curation Expert Panel; ClinGen X-Linked Inherited Retinal Disease Variant Curation Expert Panel, Genetics, Volume 232, Issue 4, April 2026, iyaf215, https://doi.org/10.1093/genetics/iyaf215

License

CC-BY 4.0

Contact

Please use this GitHub repository's Issue tracker to request new terms/classes or report errors or specific concerns related to the ontology.

Acknowledgements

This ontology repository was created using the ontology starter kit