EGFR Exon 20 Deletion Mutation

Preferred Label : EGFR Exon 20 Deletion Mutation;

NCIt synonyms : Epidermal Growth Factor Receptor Gene Exon 20 Deletion Mutation; ERBB Exon 20 Deletion Mutation; EGFR Exon 20 Gene Deletion Mutation; HER1 Exon 20 Deletion Mutation; ERBB1 Exon 20 Deletion Mutation;

NCIt definition : A molecular genetic abnormality indicating the presence of an in-frame deletion mutation occurring within exon 20 of the EGFR gene.;

NCI Metathesaurus CUI : CL951291;

Details

Origin ID

C159434;

UMLS CUI

C5204431;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
molecular_abnormality_involves_gene
- EGFR Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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