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Ontology Browser

Term:
acute myeloid leukemia, inv(16)(p13.3;q24.3) (EFO:MONDO:0100406)
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Parent Terms Term With Siblings Child Terms
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) 
Any acute myeloid leukemia that has the chromosomal anomaly inv(16)(p13.3;q24.3). (A pericentric chromosomal inversion that involves chromosome 16. It is associated with CBFA2T3/GLIS2 fusions and pediatric acute megakaryoblastic leukemia.)
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 
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 

Synonyms
Exact Synonyms: AML, inv(16)(p13.3;q24.3);  AML, inv(16)(p13.3q24.3);  AML, inv(16)(p13;q24);  AML, inv(16)(p13q24)
Alternate IDs: MONDO:0100406
Definition Sources: https://orcid.org/0000-0001-9863-851X, https://orcid.org/0000-0002-3302-4610, NCIT:C167195

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