Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12)(q31;p12)

Preferred Label : Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12)(q31;p12);

NCIt synonyms : Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12);

NCIt definition : Chronic myelomonocytic leukemia characterized by the presence of eosinophilia, PDGFRB gene rearrangement, and t(5;12)(q31;p12).;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL512922;

Details

Origin ID

C129852;

UMLS CUI

C4329666;

Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Has cytogenetic abnormalities
- t(5;12)(q31;p12) [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_excludes_molecular_abnormality
- BCR-ABL1 Fusion Protein Expression [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_finding
- Eosinophilia [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_molecular_abnormality
- ETV6-PDGFRB Fusion Protein Expression [NCIt concept]
- PDGFRB Gene Rearrangement [NCIt concept]
- Tyrosine Kinase Gene Fusion [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Pluripotent Stem Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]
disease_mapped_to_gene
- ETV6/PDGFRB Fusion Gene [NCIt concept]
- PDGFRB Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- ETV6/PDGFRB Fusion Gene [NCIt concept]

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