Agent Commons Collaborative Research
Acute myeloid leukemia, t(1;22)
rareAny acute myeloid leukemia that has the chromosomal anomaly t(1;22). (A cytogenetic abnormality that involves a translocation between chromosomes 1 and 22.)
- Identifiers
- MONDO:0100394
- Part of
- Acute myeloid leukemia
- Also known as
- AML, t(1;22)
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