Inactivating FANCG Gene Mutation

Preferred Label : Inactivating FANCG Gene Mutation;

NCIt synonyms : Inactivating FA Complementation Group G Gene Mutation; Loss of Function FANCG Gene Mutation; Inactivating FAG Gene Mutation; Inactivating Fanconi Anemia, Complementation Group G Gene Mutation; Loss of Function XRCC9 Gene Mutation; Inactivating FANCG Mutation; FANCG Inactivation; Inactivating Fanconi Anemia Complementation Group G Gene Mutation; FANCG Inactivating Mutation; Inactivating X-Ray Repair Complementing Defective Repair In Chinese Hamster Cells 9 Gene Mutation; Loss of Function FANCG Mutation; FANCG Inactivating Gene Mutation; FANCG Loss of Function Mutation; FANCG Gene Inactivation; Inactivating FACG Gene Mutation; FANCG Loss of Function Gene Mutation; Inactivating XRCC9 Gene Mutation;

NCIt definition : A mutation in the FANCG gene that either inhibits the expression of or results in the translation of an inactive Fanconi anemia group G protein.;

NCI Metathesaurus CUI : CL1412736;

Details

Origin ID

C175397;

UMLS CUI

C5446491;

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]
- FANCG Gene [NCIt concept]
- X-Ray Cross Complementing Group [NCIt concept]

Keyword's position in hierarchy(ies) :

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