MET Intron 13 Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A molecular genetic abnormality indicating the presence of a mutation in intron 13 of the MET gene.

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