Agent Commons Collaborative Research

Acute myeloid leukemia

rare

Acute myeloid leukemia (AML) is a group of neoplasms arising from precursor cells committed to the myeloid cell-line differentiation. All of them are characterized by clonal expansion of myeloid blasts. AML manifests by fever, pallor, anemia, hemorrhages and recurrent infections.

Identifiers
MONDO:0018874 OMIM:601626Orphanet:519
Part of
Acute leukemiaMyeloid leukemia
Also known as
acute granulocytic leukaemia · acute granulocytic leukemia · acute myeloblastic leukemia · acute myelocytic leukaemia · acute myelocytic leukemia

Subtypes

All diseases Rare only
Disease Subtypes
Acute myeloid leukemia by FAB classification 16
Acute leukemia of ambiguous lineage 10
Acute monocytic leukemia 3
Inherited acute myeloid leukemia 3
Therapy related acute myeloid leukemia and myelodysplastic syndrome 3
Acute myeloid leukemia with 11q23 abnormalities
Acute myeloid leukemia with BCR-ABL1
Acute myeloid leukemia with CBFA2T3-GLIS2 fusion
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with FUS-ERG fusion
Acute myeloid leukemia with MNX1-ETV6 fusion
Acute myeloid leukemia with NPM1 somatic mutations
Acute myeloid leukemia with NPM1-MLF1 fusion
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)
Acute myeloid leukemia with multilineage dysplasia
Acute myeloid leukemia with mutated NPM1
Acute myeloid leukemia with t(6;9)(p23;q34)
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute myeloid leukemia with t(9;11)(p22;q23)
Acute myeloid leukemia, CEBPA gene mutation
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, 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, MLL gene rearrangement
Acute myeloid leukemia, Monosomy 5
Acute myeloid leukemia, Monosomy 7
Acute myeloid leukemia, NRAS gene mutation
Acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive
Acute myeloid leukemia, PTPN11 gene mutation
Acute myeloid leukemia, RUNX1 gene mutation
Acute myeloid leukemia, Trisomy 8
Acute myeloid leukemia, WT1 gene mutation
Acute myeloid leukemia, biallelic CEBPA gene mutation
Acute myeloid leukemia, del(13q14-q21)
Acute myeloid leukemia, del(5q31-q32)
Acute myeloid leukemia, der12p
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, loss of chromosome 17p
Acute myeloid leukemia, monoallelic CEBPA 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(1;22)(p13;q13)
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(8;21)(q22; q22.1)
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)
Childhood acute myeloid leukemia
Core binding factor acute myeloid leukemia
Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)

Rare disease

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