EGFR Exon 20 Insertion Mutation

Preferred Label : EGFR Exon 20 Insertion Mutation;

NCIt related terms : Exon 20 Insertion;

NCIt definition : Mutation located after the C-helix of the tyrosine kinase domain of EGFR.;

Details

Origin ID

C125605;

UMLS CUI

C4086254;

See also inter- (CISMeF)
- advanced non-small cell lung cancer with activating epidermal growth factor receptor exon 20 insertion mutations [Indication]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Lung Squamous Cell Carcinoma and Lung Adenocarcinoma Baseline Form [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- EGFR Protein Variant [NCIt concept]
is_target
- EGFR Mutant-selective Inhibitor FWD1509 MsOH [NCIt concept]
- EGFR/HER2 Mutant-selective Inhibitor HS-10376 [NCIt concept]
- EGFR/HER2 Mutant-selective Inhibitor STX-721 [NCIt concept]
- Mobocertinib [NCIt concept]
- Mobocertinib Succinate [NCIt concept]
- Pebezertinib [NCIt concept]
- Sunvozertinib [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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