MET Intron 13 Mutation

Preferred Label : MET Intron 13 Mutation;

NCIt synonyms : MET Proto-Oncogene, Receptor Tyrosine Kinase Intron 13 Mutation; HGFR Intron 13 Mutation; Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Intron 13 Mutation; c-Met Intron 13 Mutation;

NCIt definition : A molecular genetic abnormality indicating the presence of a mutation in intron 13 of the MET gene.;

NCI Metathesaurus CUI : CL545067;

Details

Origin ID

C147120;

UMLS CUI

C4554232;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
molecular_abnormality_involves_gene
- MET Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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