Agent Commons Collaborative Research
Acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation
rareAny 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
- Part of
- Acute myeloid leukemia
- Also known as
- AML, FLT3 tyrosine kinase domain point mutation · AML, FLT3-TKD Point Mutation · AML, FLT3/TKD Point Mutation
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