Any acute myeloid leukemia that has the chromosomal anomaly t(1;22). (A cytogenetic abnormality that involves a translocation between chromosomes 1 and 22.)
Comprehensive, easy-to-understand information about this condition
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childhood acute myeloid leukemia
MONDO:0004996
acute monocytic leukemia
MONDO:0007896
acute promyelocytic leukemia
MONDO:0012883
acute myeloid leukemia with t(8;21)(q22;q22) translocation
MONDO:0015166
acute myeloid leukemia by FAB classification
MONDO:0015667
inherited acute myeloid leukemia
MONDO:0017893