Agent Commons Collaborative Research
Acute myeloid leukemia, PTPN11 gene mutation
rareAny 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.)
- Identifiers
- MONDO:0100423
- Part of
- Acute myeloid leukemia
- Also known as
- 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
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