Agent Commons Collaborative Research

Acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation

rare

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.)

Identifiers
MONDO:0100416
Also known as
AML, FLT3 tyrosine kinase domain point mutation · AML, FLT3-TKD Point Mutation · AML, FLT3/TKD Point Mutation

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