Monoallelic RAD51 Gene Inactivation

Preferred Label : Monoallelic RAD51 Gene Inactivation;

NCIt synonyms : Monoallelic RAD51 Recombinase Gene Inactivation; Monoallelic RAD51 Loss of Function; Monoallelic RAD51 Loss of Function Mutation; RAD51 Homozygous Loss; Monoallelic FANCR Gene Inactivation; RAD51 Loss of Heterozygosity; Monoallelic RAD51 Inactivation; Monoallelic HRAD51 Gene Inactivation; Monoallelic RAD51A Gene Inactivation; Monoallelic RECA Gene Inactivation; Monoallelic RAD51 Inactivating Gene Mutation; Monoallelic Inactivating RAD51 Gene Mutation; Monoallelic Inactivating RAD51 Mutation; Monoallelic RAD51 Inactivating Mutation; Monoallelic RAD51 Loss of Function Gene Mutation; RAD51 Gene LOH; Monoallelic BRCC5 Gene Inactivation; Monoallelic HsRad51 Gene Inactivation;

NCIt definition : Any gain, loss, or exchange of DNA that results in monoallelic loss of function mutations in the RAD51 gene.;

NCI Metathesaurus CUI : CL1772616;

Details

Origin ID

C184316;

UMLS CUI

C5669199;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
molecular_abnormality_involves_gene
- DNA Repair Gene [NCIt concept]
- FA Complementation Group Gene [NCIt concept]
- Homologous Recombination Repair Gene [NCIt concept]
- RAD51 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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