FLT3 Tyrosine Kinase Domain Point Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** Single nucleotide mutations in the tyrosine kinase domain encoded by the human FLT3 gene that are associated with acute myeloid leukemia and poor prognosis.

**Synonyms:** - FLT3-TKD Point Mutation - FLT3/TKD Point Mutation