| Preferred Name |
Molecular Abnormality |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3910 |
| code |
C3910 |
| DEFINITION |
A molecular or cytogenic abnormality which occurs in either human disease states or disease models. |
| FULL_SYN |
Cytogenetic or Molecular Genetic Abnormality Chromosomal, Gene, or Protein Abnormality Genetic Abnormality |
| label |
Molecular Abnormality |
| Legacy_Concept_Name |
Molecular_Abnormality |
| NCI_META_CUI |
CL448235 |
| Preferred_Name |
Molecular Abnormality |
| prefixIRI |
C3910 |
| prefLabel |
Molecular Abnormality |
| Semantic_Type |
Cell or Molecular Dysfunction |
| subClassOf | |
| disjointWith |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97325 |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||