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Acute Myeloid Leukemia, Ptpn11 Gene Mutation (MONDO:0100423)

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.)

Overview

Category

musculoskeletal system disorder

connective tissue disorder

immune system disorder

hematologic disorder

Ontology ID

MONDO:0100423

Internal:24150

Synonyms

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

AML, SHP2 Gene Mutation

Mapped terms

GARD:0026206

Child terms

Unknown children.

Results

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