Acute myeloid leukemia, CEBPA gene mutation

Any acute myeloid leukemia that has the chromosomal anomaly CEBPA gene mutation. (Mutation of the CEBPA gene encoding CCAAT/enhancer binding protein alpha. It is seen in acute myeloid leukemias usually associated with a normal karyotype.)

Also known as: AML, C/EBP-Alpha Gene Mutation, AML, C/EBPalpha Mutation, AML, CCAAT Enhancer Binding Protein Alpha Gene Mutation, AML, CCAAT/Enhancer Binding Protein, Alpha Gene Mutation, AML, CEBP Gene Mutation, AML, CEBPA Mutation, AML, CEBPA gene mutation

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, CEBPA gene mutation itself.