Orphanet Rare Diseases Ontology in OBO (deprecated) (ORDO_OBO)
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This is the OBO version of the Orphanet Rare Disease ontology (ORDO) which is jointly developed...
Ontology Info
| Field | Value |
|---|---|
| Acronyme | ORDO_OBO |
| Description | This is the OBO version of the Orphanet Rare Disease ontology (ORDO) which 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. <br><br>It derived from the Orphanet database (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). |
| Format | OBO |
| Categories | Health, Biomedical Resources, Human, Phenotype |
| Groups |
Metrics
| Metric | Value |
|---|---|
| Classes | 11,699 |
| Individuals | 0 |
| Properties | 12 |
| Max Depth | 11 |
| Max Child Count | 3,408 |
| Average Child Count | 13 |
| Classes With One Child | 294 |
| Classes With More Than 25 Children | 11 |
| Classes With No Definition | 11,699 |
Projects using ORDO_OBO
No projects using ORDO_OBO
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