C82612Level 5
PTPN11 Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** Mutation of the protein tyrosine phosphatase, non-receptor type 11 gene. It is seen in cases of juvenile myelomonocytic leukemia.
**Synonyms:** - BPTP3 Gene Mutation - PTP-1D Gene Mutation - PTP2C Gene Mutation - PTPN11 - PTPN11 Mutation - Protein Tyrosine Phosphatase Non-Receptor Type 11 Gene Mutation - Protein Tyrosine Phosphatase, Non-Receptor Type 11 Gene Mutation - SH-PTP2 Gene Mutation - SHP-2 Gene Mutation - SHP2 Gene Mutation
GET
/api/v1/systems/nci_thesaurus/nodes/C82612Hierarchy Explorer
Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.