Acute myeloid leukemia, t(16;21)(p11;q22)

MONDO:0100410

Any acute myeloid leukemia that has the chromosomal anomaly t(16;21)(p11;q22). (A chromosomal translocation involving the FUS gene on chromosome 16p11 and the ERG gene on chromosome 21q22.)

Also known as: AML, t(16;21)(p11.2;q22.2), AML, t(16;21)(p11;q22)

3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(16;21)(p11;q22) itself.

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↑ Acute myeloid leukemia (1192)

Including sub-types (3080) Tagged with Acute myeloid leukemia, t(16;21)(p11;q22) (0)

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