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Mondo Disease Ontology
Last uploaded:
January 7, 2025
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| Preferred Name | biotin metabolic disease | |
| Synonyms | ||
| Definitions |
A deficiency in biotin through either inherited or acquired causes. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0020699 |
|
| database_cross_reference |
UMLS:C2937225 MEDGEN:754289
|
|
| definition |
A deficiency in biotin through either inherited or acquired causes.
|
|
| id |
MONDO:0020699
|
|
| label |
biotin metabolic disease
|
|
| notation |
MONDO:0020699
|
|
| prefLabel |
biotin metabolic disease
|
|
| skos_exactMatch | ||
| treeView | ||
| subClassOf |
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| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
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| Mapping To | Ontology | Source |
|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0020699 | CCONT | SAME_URI |
| http://purl.obolibrary.org/obo/MONDO_0020699 | DOVES | SAME_URI |
| http://purl.obolibrary.org/obo/MONDO_0020699 | EFO | SAME_URI |
| http://purl.obolibrary.org/obo/MONDO_0020699 | CCONT | LOOM |
| http://purl.obolibrary.org/obo/MONDO_0020699 | DOVES | LOOM |
| http://purl.obolibrary.org/obo/MONDO_0020699 | EFO | LOOM |