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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
acute erythroblastic leukemia 
acute leukemia of ambiguous lineage +  
An acute leukemia in which the blasts lack sufficient evidence to classify as myeloid or lymphoid or they have morphologic and/or immunophenotypic characteristics of both myeloid and lymphoid cells. (WHO, 2001)
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 
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: acute leukaemia of indeterminate lineage;  acute leukemia of indeterminate lineage;  hybrid acute leukaemia;  hybrid acute leukemia;  mixed lineage acute leukaemia;  mixed lineage acute leukemia
Related Synonyms: ALL with myeloid markers;  AML with lymphoid markers;  BAL;  acute leukaemia of undetermined lineage;  acute leukemia of undetermined lineage;  biphenotypic acute leukaemia;  biphenotypic acute leukemia;  mixed phenotype acute leukaemia;  mixed phenotype acute leukemia
Alternate IDs: MONDO:0019460
Xrefs: GARD:8638;  MEDGEN:226983;  MedDRA:10067399;  NANDO:2200017;  NANDO:2200018;  NCI:C7464;  ORDO:86851;  SCTID:721308005;  UMLS:C1301357;  icd11.foundation:1062906118
Definition Sources: NCIT:C7464

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