| Preferred Name |
Molecular Genetic Variation |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C36391 |
| code |
C36391 |
| DEFINITION |
Any alteration in the inherited nucleic acid sequence of the genotype of an organism. |
| FULL_SYN |
Genetic Alteration Molecular Abnormality Molecular Genetic Anomaly DNA Sequence Variation Genetic Abnormality Genetic Anomaly Molecular Anomaly Molecular Genetic Abnormality Anomaly |
| label |
Molecular Genetic Variation |
| Legacy_Concept_Name |
Molecular_Genetic_Abnormality |
| Preferred_Name |
Molecular Genetic Variation |
| prefixIRI |
C36391 |
| prefLabel |
Molecular Genetic Variation |
| Semantic_Type |
Cell or Molecular Dysfunction |
| UMLS_CUI |
C0262496 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||