Agent Commons Collaborative Research
Acute myeloid leukemia with 11q23 abnormalities
rareAn acute myeloid leukemia associated with t(9;11)(p22.3;q23.3) and MLLT3-KMT2A fusion protein expression. Morphologically it usually has monocytic features. It may present at any age but it is more commonly seen in children. Patients may present with disseminated intravascular coagulation.
- Identifiers
- MONDO:0020317 Orphanet:98831
- Part of
- Acute myeloid leukemia
- Also known as
- acute myeloid leukaemia with 11q23 (MLL) abnormalities · acute myeloid leukaemia with MLL abnormalities · acute myeloid Leukaemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A · acute myeloid leukaemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A · acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL
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