Any acute myeloid leukemia that has the chromosomal anomaly PTPN11 gene mutation. (Mutation of the protein tyrosine phosphatase, non-receptor type 11 gene. It is seen in cases of juvenile myelomonocytic leukemia.). The disease is acute myeloid leukemia, PTPN11 gene mutation (MONDO_0100423). Also known as: AML, BPTP3 Gene Mutation, AML, PTP-1D Gene Mutation, AML, PTP2C Gene Mutation, AML, PTPN11 gene mutation, AML, Protein Tyrosine Phosphatase Non-Receptor Type 11 Gene Mutation, AML, Protein Tyrosine Phosphatase, Non-Receptor Type 11 Gene Mutation, AML, SH-PTP2 Gene Mutation, AML, SHP-2 Gene Mutation.