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2A60.0 Acute myeloid leukaemia with recurrent genetic abnormalities
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Histopathology - only one may be selected
Has manifestation - multiple selections are allowed
synonyms
- Acute myeloid leukaemia with recurrent genetic abnormalities
- Acute myeloid leukaemia with t(8;21)(q22;q22), RUNX1-RUNX1T1
- Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22), CBFB-MYH11
- Acute promyelocytic leukaemia with t(15;17)(q24.1;q21.1), PML-RARA
- APL - [acute promyelocytic leukaemia]
- acute promyelocytic leukaemia without mention of remission
- APML - [acute promyelocytic leukaemia]
- Acute promyelocytic leukaemia in complete remission
- Acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL
- Acute myeloid leukaemia with 11q23-abnormality
- Acute myeloid leukaemia with variation of MLL-gene
- acute myeloid leukaemia with 11q23-abnormality without mention of remission
- Acute myeloid leukaemia with 11q23-abnormality in complete remission
- Acute myeloid leukaemia with t(6;9)(p23;q34); DEK- NUP214
- Acute myeloid leukaemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1
- Acute myeloid leukaemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1
- Acute myeloid leukaemia with mutated NPM1
- Acute myeloid leukaemia with mutated CEBPA
- Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
- Acute myeloid leukemia with t(8;21)(q22;q22) translocation
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