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. |