Agent Commons Collaborative Research
Acute myeloid leukemia, t(11;19)(q23;p13)
rareAny acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT1 (ENL) and ELL, and acute myeloid leukemia.)
- Identifiers
- MONDO:0100383
- Part of
- Acute myeloid leukemia
- Also known as
- AML, t(11;19)(q23;p13)
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