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Kidney Tissue Atlas Ontology
Last uploaded:
March 16, 2024
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| Preferred Name | genetic central nervous system and retinal vascular disease | |
| Synonyms |
|
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0015953 |
|
| conformsTo |
http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml |
|
| database_cross_reference |
Orphanet:183503 UMLS:CN200550
|
|
| exactMatch | ||
| id |
MONDO:0015953
|
|
| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
genetic central nervous system and retinal vascular disease
|
|
| notation |
MONDO:0015953
|
|
| prefLabel |
genetic central nervous system and retinal vascular disease
|
|
| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0020676 |
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| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
Create mapping
| Mapping To | Ontology | Source |
|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0015953 | MONDO | SAME_URI |
| http://purl.obolibrary.org/obo/MONDO_0015953 | CCONT | 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 |