Agent Commons Collaborative Research
Acute myeloid leukemia, t(15;17)(q24;q21)
rareAny acute myeloid leukemia that has the chromosomal anomaly t(15;17)(q24;q21). (A chromosomal translocation associated with creation of a fusion between the PML and RARA genes. It is seen in variants of acute promyelocytic leukemia.)
- Identifiers
- MONDO:0100375
- Part of
- Acute myeloid leukemia
- Also known as
- AML, t(15;17)(q22;q12) · AML, t(15;17)(q22;q21) · AML, t(15;17)(q24;q21)
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