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loading...| Preferred Name |
genetic central nervous system and retinal vascular disease |
|
| Synonyms |
|
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0015953 |
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| conformsTo |
http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml |
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| database_cross_reference |
Orphanet:183503 UMLS:CN200550 |
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| exactMatch | ||
| id |
MONDO:0015953 |
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| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
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| label |
genetic central nervous system and retinal vascular disease |
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| notation |
MONDO:0015953 |
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| prefLabel |
genetic central nervous system and retinal vascular disease |
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| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0020676 |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0015953 | MONDO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0015953 | EFO | SAME_URI | |
| http://www.orpha.net/ORDO/Orphanet_183503 | ORDO | LOOM | |
| http://www.limics.org/hrdo/rdfns#pat_id_18254 | HRDO | LOOM | |
| http://www.orpha.net/ORDO/Orphanet_183503 | ORDO | LOOM |