ols/orphanet.ordo: for: orphanet.ordo type: synonym orphanet.ordo: alias: 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. It 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). forward: https://www.ebi.ac.uk/ols/ontologies/ordo/terms?short_form=${ac} institution: European Bioinformatics Institute, Hinxton, Cambridge location: UK more: https://www.ebi.ac.uk/ols/ontologies/ordo name: ORDO via OLS pattern: ^Orphanet(_|:)C?\d+$ prefixed: false primary: true probe: https://www.ebi.ac.uk/ols/ontologies/ordo/terms?short_form=Orphanet_C023 provider: ols provider_id: MIR:00100705 redirect: https://www.ebi.ac.uk/ols/ontologies/ordo/terms?short_form=$id sort_score: 6 state: 99:Up subject: ontology; disease synonym: ORDO test: Orphanet_C023 type: scheme