Acute myeloid leukemia, t(11;17)

MONDO:0100392

Any acute myeloid leukemia that has the chromosomal anomaly t(11;17). (A cytogenetic abnormality that involves a translocation between chromosomes 11 and 17.)

Also known as: AML, t(11;17)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(11;17) itself.

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↑ Acute myeloid leukemia (1194)

Including sub-types (3091) Tagged with Acute myeloid leukemia, t(11;17) (0)

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