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loading...| Preferred Name | obsolete genetic central nervous system and retinal vascular disease | |
| Synonyms |
|
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0015953 |
|
| Obsolete |
true |
|
| consider |
MONDO:0005071 |
|
| database_cross_reference |
Orphanet:183503 |
|
| deprecated |
true |
|
| IAO_0000231 | ||
| IAO_0000233 | ||
| id |
MONDO:0015953 |
|
| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_group_of_disorders |
|
| label |
obsolete genetic central nervous system and retinal vascular disease |
|
| notation |
MONDO:0015953 |
|
| preferred label |
obsolete genetic central nervous system and retinal vascular disease |
|
| prefLabel |
obsolete genetic central nervous system and retinal vascular disease |
|
| skos_exactMatch |
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://purl.obolibrary.org/obo/MONDO_0015953 | KTAO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0015953 | MONDO | LOOM | |
| http://www.orpha.net/ORDO/Orphanet_183503 | EFO | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0015953 | EFO | LOOM |