Acute myeloid leukemia, PTPN11 gene mutation
From BugSigDB
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.)
- Aliases
- AML, BPTP3 Gene Mutation
- AML, Protein Tyrosine Phosphatase Non-Receptor Type 11 Gene Mutation
- AML, Protein Tyrosine Phosphatase, Non-Receptor Type 11 Gene Mutation
- AML, PTP-1D Gene Mutation
- AML, PTP2C Gene Mutation
- AML, PTPN11 gene mutation
- AML, SH-PTP2 Gene Mutation
- AML, SHP-2 Gene Mutation
- AML, SHP2 Gene Mutation