C96861Level 7
EGFR-TKI Sensitizing Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A molecular genetic abnormality indicating the presence of a sensitizing mutation in the epidermal growth factor receptor-tyrosine kinase inhibitor domain.
**Synonyms:** - EGFR Mutation Resulting in Tyrosine Kinase Inhibitor Sensitivity - EGFR Tyrosine Kinase Inhibitor Sensitizing Mutation
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