Acute myeloid leukemia, CEBPA gene mutation

MONDO:0100414

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

3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, CEBPA gene mutation itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by

Showing the 400 most recently updated of 595 trials in this tab.