Acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation

Definition

Any acute myeloid leukemia that has the chromosomal anomaly FLT3 tyrosine kinase domain point mutation. (Single nucleotide mutations in the tyrosine kinase domain encoded by the human FLT3 gene that are associated with acute myeloid leukemia and poor prognosis.)

Also known as AML, FLT3 tyrosine kinase domain point mutation, AML, FLT3-TKD Point Mutation, AML, FLT3/TKD Point Mutation — per MONDO