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. |