Terminology Service for NFDI4Health
EGFR-TKI Sensitizing Mutation
Go to external page
http://purl.obolibrary.org/obo/NCIT_C96861
A molecular genetic abnormality indicating the presence of a sensitizing mutation in the epidermal growth factor receptor-tyrosine kinase inhibitor domain. [ ]
Term info
Label
EGFR-TKI Sensitizing Mutation
Synonyms
- EGFR Mutation Resulting in Tyrosine Kinase Inhibitor Sensitivity
- EGFR Tyrosine Kinase Inhibitor Sensitizing Mutation
- EGFR-TKI Sensitizing Mutation
Subsets
NCIT_C116977, NCIT_C142800, NCIT_C142799
Contributing Source
CTRP
Display Name
EGFR-TKI Sensitizing Mutation
Preferred Name
EGFR-TKI Sensitizing Mutation
Semantic Type
Cell or Molecular Dysfunction
UMLS CUI
C3273083
code
C96861