Measures Concepts
GitHub icon <>

AML with Recurrent Genetic Abnormalities

AML with Recurrent Genetic Abnormalities is a type of Acute Myeloid Leukemia

Subtypes of AML with Recurrent Genetic Abnormalities include AML (megakaryoblastic) with t(1;22)(p13.3;q13.3);RBM15-MKL1, AML with BCR-ABL1, AML with Biallelic Mutations of CEBPA, AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22);CBFB-MYH11, AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM, AML with Mutated NPM1, AML with Mutated RUNX1, AML with t(6;9)(p23;q34.1);DEK-NUP214, AML with t(8;21)(q22;q22.1);RUNX1-RUNX1T1, AML with t(9;11)(p21.3;q23.3);MLLT3-KMT2A, APL with PML-RARA

title AML with Recurrent Genetic Abnormalities type cancerType mainType Leukemia tissue Myeloid oncoTreeId AMLRGA parentOncoTreeId AML oncoTreeLevel 4 subTypes 11

View source

#CancerMoonshot Search Add Concept About Blog Acknowledgements Queries Stats Sponsor Day 369 manager@cancerdb.com 1-808-727-1111