loading...| Preferred Name | genetic otorhinolaryngologic disease | |
| Synonyms |
genetic otorhinolaryngologic disease |
|
| Definitions |
An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome. Reason: out of scope. MONDO:excludeGeneticFormOfDisease and MONDO:excludeGroupingClass. Term to consider: MONDO:0024623 otorhinolaryngologic disease |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0018751 |
|
| comment |
Reason: out of scope. MONDO:excludeGeneticFormOfDisease and MONDO:excludeGroupingClass. Term to consider: MONDO:0024623 otorhinolaryngologic disease |
|
| altLabel |
genetic otorhinolaryngologic disease |
|
| definition |
An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome. Reason: out of scope. MONDO:excludeGeneticFormOfDisease and MONDO:excludeGroupingClass. Term to consider: MONDO:0024623 otorhinolaryngologic disease |
|
| has characteristic | ||
| has_exact_synonym |
genetic otorhinolaryngologic disease |
|
| IAO_0000233 | ||
| IAO_0006012 |
2022-09-01 |
|
| label |
genetic otorhinolaryngologic disease |
|
| prefixIRI |
MONDO:0018751 |
|
| prefLabel |
genetic otorhinolaryngologic disease |
|
| textual definition |
An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome. |
|
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0018751 | GCBO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0018751 | CCONT | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0018751 | EFO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0018751 | MONDO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0018751 | EFO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0018751 | KTAO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0018751 | OBA | SAME_URI | |
| http://www.orpha.net/ORDO/Orphanet_466084 | ORDO | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0018751 | KTAO | LOOM |