| Preferred Name |
Inclusion Body |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C120945 |
| ALT_DEFINITION |
A general term used to describe abnormal structures present within the cytoplasm or nucleus of a cell. (INHAND) |
| code |
C120945 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C61410 |
| Contributing_Source |
CDISC |
| DEFINITION |
A detectable aggregation of substance in the cytoplasm or nucleus. |
| FULL_SYN |
Inclusion Bodies Inclusions INCLUSION |
| label |
Inclusion Body |
| Preferred_Name |
Inclusion Body |
| prefixIRI |
C120945 |
| prefLabel |
Inclusion Body |
| Semantic_Type |
Finding |
| UMLS_CUI |
C0007637 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/GO_0016234 | Human Phenotype Ontology China | LOOM | |
| http://purl.obolibrary.org/obo/GO_0016234 | Gene Ontology | LOOM |