Monoallelic RAD51D Gene Inactivation

Preferred Label : Monoallelic RAD51D Gene Inactivation;

NCIt synonyms : Monoallelic Inactivating RAD51D Gene Mutation; Monoallelic RAD51D Inactivating Gene Mutation; Monoallelic RAD51 Paralog D Gene Inactivation; Monoallelic R51H3 Gene Inactivation; Monoallelic RAD51D Loss of Function Gene Mutation; RAD51D Loss of Heterozygosity; RAD51D Homozygous Loss; Monoallelic RAD51D Inactivating Mutation; Monoallelic Inactivating RAD51D Mutation; Monoallelic RAD51-Like 3 Gene Inactivation; Monoallelic RAD51D Loss of Function; Monoallelic RAD51 Homolog D Gene Inactivation; Monoallelic RAD51D Loss of Function Mutation; Monoallelic RAD51L3 Gene Inactivation; Monoallelic BROVCA4 Gene Inactivation; RAD51D Gene LOH; Monoallelic RAD51D Inactivation; Monoallelic TRAD Gene Inactivation;

NCIt definition : Any gain, loss, or exchange of DNA that results in monoallelic loss of function mutations in the RAD51D gene.;

NCI Metathesaurus CUI : CL1772627;

Details

Origin ID

C184320;

UMLS CUI

C5669203;

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]
- Homologous Recombination Repair Gene [NCIt concept]
- RAD51D Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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