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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Genetic central nervous system and retinal vascular disease | |
| Synonyms |
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| ID |
http://www.orpha.net/ORDO/Orphanet_183503 |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=183503 |
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| hasDbXref |
UMLS:C5681839
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| label |
Genetic central nervous system and retinal vascular disease
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| notation |
ORPHA:183503 Category
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| prefixIRI |
ORDO:Orphanet_183503
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| prefLabel |
Genetic central nervous system and retinal vascular disease
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| subClassOf |
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| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
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| Mapping To | Ontology | Source |
|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_183503 | CCONT | SAME_URI |
| http://www.orpha.net/ORDO/Orphanet_183503 | EFO | SAME_URI |
| http://www.limics.org/hrdo/rdfns#pat_id_18254 | HRDO | LOOM |
| http://purl.obolibrary.org/obo/MONDO_0015953 | KTAO | LOOM |