Orphanet Rare Diseases Ontology
Names
More detailed information about this field from each metasource.
Orphanet Rare Diseases Ontology
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
ORDO
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
metasource: Biontology / Bioportal
version: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
Orphanet Rare Disease Ontology
metasource: Biontology / Bioportal
version: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
ordo
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
Names
More detailed information about this field from each metasource.
Orphanet Rare Diseases Ontology
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
ORDO
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
metasource: Biontology / Bioportal
version: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
Orphanet Rare Disease Ontology
metasource: Biontology / Bioportalversion: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
ordo
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
Other names: ORDO, Orphanet Rare Disease Ontology, ordo
Names
More detailed information about this field from each metasource.
Orphanet Rare Diseases Ontology
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
ORDO
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
metasource: Biontology / Bioportal
version: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
Orphanet Rare Disease Ontology
metasource: Biontology / Bioportalversion: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
ordo
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
Orphanet Rare Diseases Ontology (ORDO) provide 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.
Description
More detailed information about this field from each metasource.
Orphanet Rare Diseases Ontology (ORDO) provide 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.
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
The Orphanet Rare Disease ontology (ORDO) is jointly developed by Orphanet and the EBI to provide 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 derived from the Orphanet database (www.orpha.net <http://www.orpha.net>) , a multilingual database dedicated to rare diseases populated from literature and validated by international experts. It integrates a nosology (classification of rare diseases), relationships (gene-disease relations, epiemological data) and connections with other terminologies (MeSH, SNOMED CT, UMLS, MedDRA),databases (OMIM, UniProtKB, HGNC, ensembl, Reactome, IUPHAR, Geantlas) or classifications (ICD10). The ontology will be maintained by Orphanet and further populated with new data. Orphanet classifications can be browsed in the OLS view. The Orphanet Rare Disease Ontology is updated monthly and follows the OBO guidelines on deprecation of terms. It constitutes the official ontology of rare diseases produced and maintained by Orphanet (INSERM, US14).
metasource: Biontology / Bioportalversion: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
The Orphanet Rare Disease Ontology (ORDO) - structured vocabulary for rare diseases, capturing relationships between diseases, genes and other relevant features. It integrates a 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).
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
Webpage:
http://www.orphadata.org/cgi-bin/inc/ordo_orphanet.inc.phpWebpage
More detailed information about this field from each metasource.
http://www.orphadata.org/cgi-bin/inc/ordo_orphanet.inc.php
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
https://www.orpha.net
metasource: Biontology / Bioportalversion: 4.1 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/ORDO
http://www.ebi.ac.uk/ols/ontologies/ordo
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
Licence:
Name: Creative Commons Attribution 4.0 International (CC BY 4.0)Licence name
More detailed information about this field from each metasource.
Creative Commons Attribution 4.0 International (CC BY 4.0)
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
Apache-2.0
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
Licence URL
More detailed information about this field from each metasource.
https://creativecommons.org/licenses/by/4.0/
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
Publications:
Publications
More detailed information about this field from each metasource.
Rare diseases knowledge management: the contribution of proximity measurements in OntoOrpha and OMIM
PMID: 22874158
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
http://dx.doi.org/10.1093/bioinformatics/btw170
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
Publications
More detailed information about this field from each metasource.
Rare diseases knowledge management: the contribution of proximity measurements in OntoOrpha and OMIM
PMID: 22874158
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
http://dx.doi.org/10.1093/bioinformatics/btw170
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
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Rare diseases knowledge management: the contribution of proximity measurements in OntoOrpha and OMIM
PubMed citations: 2.
2 articles citing: Rare diseases knowledge management: the contribution of proximity measurements in OntoOrpha and OMIM
LORD: a phenotype-genotype semantically integrated biomedical data tool to support rare disease diagnosis coding in health information systems. PMID:26958175
A population-based registry as a source of health indicators for rare diseases: the ten-year experience of the Veneto Region's rare diseases registry. PMID:24646171 - http://dx.doi.org/10.1093/bioinformatics/btw170
Tags:
Tags
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diagnosis
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
disease
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
gene
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
phenotype
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
rare disease
metasource: Fairsharing.org
version: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
ontology and terminology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
pathology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
computational biology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
data quality management
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
rare diseases
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:55.574066
Tags
More detailed information about this field from each metasource.
diagnosis
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
disease
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
gene
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
phenotype
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
rare disease
metasource: Fairsharing.orgversion: FAIRsharing.org: ORDO; Orphanet Rare Diseases Ontology; DOI: https://doi.org/10.25504/FAIRsharing.pbbnwa; Last edited: Dec. 16, 2019, 4:47 p.m.; Last accessed: Jan 03 2022 7:12 p.m.
ontology and terminology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
pathology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
computational biology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
data quality management
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
rare diseases
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:55.574066
diagnosis disease gene phenotype rare disease ontology and terminology pathology computational biology data quality management rare diseases
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