{"id":"orphanet.ordo","reasoner":"none","oboSlims":false,"is_foundary":false,"ontology_purl":"http://www.orphadata.org/data/ORDO/ordo_orphanet.owl","creator":["Marc Hanauer"],"preferredPrefix":"orphanet.ordo","title":"Orphanet Rare Disease Ontology","description":"The Orphanet Rare Disease ontology (ORDO) is a structured vocabulary for rare diseases, capturing relationships between diseases, genes and other relevant features which will form a useful resource for the computational analysis of rare diseases.\nIt integrates a nosology (classification of rare diseases), relationships (gene-disease relations, epiemological data) and connections with other terminologies (MeSH, UMLS, MedDRA), databases (OMIM, UniProtKB, HGNC, ensembl, Reactome, IUPHAR, Geantlas) and classifications (ICD10). Licensed under CC-BY-4.0.","uri":"https://www.orpha.net","homepage":"https://www.orpha.net","mailing_list":"marc.hanauer@inserm.fr","label_property":"https://www.w3.org/2000/01/rdf-schema#label","definition_property":["http://purl.org/dc/terms/description"],"synonym_property":["http://www.geneontology.org/formats/oboInOwl#hasExactSynonym","http://www.geneontology.org/formats/oboInOwl#hasNarrowSynonym","http://www.geneontology.org/formats/oboInOwl#hasBroadSynonym","http://www.geneontology.org/formats/oboInOwl#hasCloseSynonym"],"hierarchical_property":["https://www.w3.org/2000/01/rdf-schema#subClassOf"],"hidden_property":[],"base_uri":["http://www.orpha.net/ORDO/Orphanet_"]}