| Parent Terms |
Term With Siblings |
Child Terms |
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acute erythroblastic leukemia
acute leukemia of ambiguous lineage +
acute monocytic leukemia +
acute myeloid leukemia by FAB classification +
acute myeloid leukemia with CEBPA somatic mutations
acute myeloid leukemia with multilineage dysplasia
acute myeloid leukemia with mutated NPM1
acute myeloid leukemia, biallelic CEBPA gene mutation
acute myeloid leukemia, CEBPA gene mutation
acute myeloid leukemia, del(13q14-q21)
acute myeloid leukemia, del(5q31-q32)
acute myeloid leukemia, der12p
acute myeloid leukemia, FLT3 internal tandem duplication
acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation
acute myeloid leukemia, GATA1 gene mutation
acute myeloid leukemia, inv(16)(p13.1;q22)
acute myeloid leukemia, inv(16)(p13.3;q24.3)
acute myeloid leukemia, inv(3)(q21.3;q26.2)
acute myeloid leukemia, KIT exon 17 mutation
acute myeloid leukemia, KIT exon 8 mutation
acute myeloid leukemia, KIT gene mutation
acute myeloid leukemia, KRAS gene mutation
acute myeloid leukemia, loss of chromosome 17p
acute myeloid leukemia, MLL gene rearrangement Any acute myeloid leukemia that has the chromosomal anomaly MLL gene rearrangement. (A molecular abnormality indicating rearrangement of the MLL (KMT2A) gene.)
acute myeloid leukemia, monoallelic CEBPA gene mutation
acute myeloid leukemia, Monosomy 5
acute myeloid leukemia, Monosomy 7
acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive
acute myeloid leukemia, NRAS gene mutation
acute myeloid leukemia, PTPN11 gene mutation
acute myeloid leukemia, RUNX1 gene mutation
acute myeloid leukemia, t(10;11)(p11.2;q23)
acute myeloid leukemia, t(10;11)(p12;q23)
acute myeloid leukemia, t(11;15)(p15;q35)
acute myeloid leukemia, t(11;17)
acute myeloid leukemia, t(11;19)(q23.3;p13.3)
acute myeloid leukemia, t(11;19)(q23;p13)
acute myeloid leukemia, t(11;19)(q23;p13.1)
acute myeloid leukemia, t(15;17)(q24;q21)
acute myeloid leukemia, t(16;16)(p13.1;q22)
acute myeloid leukemia, t(16;21)(p11;q22)
acute myeloid leukemia, t(16;21)(q24;q22)
acute myeloid leukemia, t(1;11)(q21;q23)
acute myeloid leukemia, t(1;22)
acute myeloid leukemia, t(2;12)
acute myeloid leukemia, t(3;12)(q23;p12.3)
acute myeloid leukemia, t(3;3)(q21.3;q26.2)
acute myeloid leukemia, t(3;5)(q25;q34)
acute myeloid leukemia, t(4;11)(q21;q23)
acute myeloid leukemia, t(5;11)(q35;p15)
acute myeloid leukemia, t(6;11)(q27;q23)
acute myeloid leukemia, t(6;9)(p23;q34.1)
acute myeloid leukemia, t(7;12)(q36;p13)
acute myeloid leukemia, t(8;16)
acute myeloid leukemia, t(9;11)(p21.3;q23.3)
acute myeloid leukemia, t(9;22)(q34.1;q11.2)
acute myeloid leukemia, t(v;11q23.3)
acute myeloid leukemia, Trisomy 8
acute myeloid leukemia, WT1 gene mutation
acute promyelocytic leukemia
adult acute myeloid leukemia
childhood acute myeloid leukemia
core binding factor acute myeloid leukemia
inherited acute myeloid leukemia +
therapy related acute myeloid leukemia and myelodysplastic syndrome
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| Synonyms |
| Exact Synonyms: |
AML, KMT2A Gene Rearrangement; AML, KMT2A Rearrangement; AML, Lysine (K)-Specific Methyltransferase 2A Gene Rearrangement; AML, Lysine Methyltransferase 2A Gene Rearrangement; AML, MLL Rearrangement; AML, MLL gene rearrangement; AML, Mixed Lineage Leukaemia Gene Rearrangement; AML, Mixed Lineage Leukemia Gene Rearrangement; AML, Myeloid/Lymphoid Leukaemia Gene Rearrangement; AML, Myeloid/Lymphoid Leukemia Gene Rearrangement
; AML, Myeloid/Lymphoid or Mixed Lineage Leukaemia Gene Rearrangement; AML, Myeloid/Lymphoid or Mixed Lineage Leukemia Gene Rearrangement; AML, Myeloid/Lymphoid or Mixed-Lineage Leukaemia (Trithorax Homolog, Drosophila) Gene Rearrangement; AML, Myeloid/Lymphoid or Mixed-Lineage Leukemia (Trithorax Homolog, Drosophila) Gene Rearrangement
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| Alternate IDs: |
MONDO:0100404
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| Xrefs: |
DOID:0081094; NCI:C174129 |
| Definition Sources: |
https://orcid.org/0000-0001-9863-851X, https://orcid.org/0000-0002-3302-4610, NCIT:C122623 |
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