Monoallelic RAD51C Gene Inactivation

Preferred Label : Monoallelic RAD51C Gene Inactivation;

NCIt synonyms : Monoallelic Inactivating RAD51C Mutation; Monoallelic Inactivating RAD51C Gene Mutation; Monoallelic RAD51C Loss of Function; Monoallelic RAD51 Paralog C Gene Inactivation; Monoallelic FANCO Gene Inactivation; Monoallelic RAD51C Inactivating Mutation; RAD51C Homozygous Loss; RAD51C Gene LOH; Monoallelic RAD51C Inactivation; Monoallelic RAD51 Homolog C Gene Inactivation; Monoallelic RAD51C Inactivating Gene Mutation; Monoallelic RAD51C Loss of Function Mutation; Monoallelic RAD51L2 Gene Inactivation; Monoallelic BROVCA3 Gene Inactivation; Monoallelic RAD51C Loss of Function Gene Mutation; RAD51C Loss of Heterozygosity;

NCIt definition : Any gain, loss, or exchange of DNA that results in monoallelic loss of function mutations in the RAD51C gene.;

NCI Metathesaurus CUI : CL1772629;

Details

Origin ID

C184318;

UMLS CUI

C5669201;

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]
- RAD51C Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients