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Acute myeloid leukemia, inv(3)(q21.3;q26.2)

MONDO:0100398

Any acute myeloid leukemia that has the chromosomal anomaly inv(3)(q21.3;q26.2). (A cytogenetic abnormality that refers to a paracentric inversion involving breakpoints on the long (q23.1 and q26.2) of chromosome 3. It is associated with acute myeloid leukemia.)

Also known as: AML, inv(3)(q21.3;q26.2), AML, inv(3)(q21.3q26.2), AML, inv(3)(q21q26.2)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, inv(3)(q21.3;q26.2) itself.

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