Myeloid/Lymphoid Neoplasms with PDGFRB Rearrangement

Preferred Label : Myeloid/Lymphoid Neoplasms with PDGFRB Rearrangement;

NCIt synonyms : Myeloid Neoplasms with PDGFRB Rearrangement; Myeloid and Lymphoid Neoplasms with PDGFRB Rearrangement; M/LN-eo with PDGFRB Rearrangement; Myeloid/Lymphoid Neoplasm with PDGFRB Rearrangement;

NCIt definition : Myeloid and rarely lymphoid neoplasms characterized by the rearrangement of the PDGFRB gene, most often resulting in the formation of ETV6-PDGFRB fusion transcripts. Patients usually present with chronic myelomonocytic leukemia and less often with atypical chronic myeloid leukemia, or chronic eosinophilic leukemia.;

Neoplastic status : Malignant;

ICD-O code : 9966/3;

Details

Origin ID

C84276;

UMLS CUI

C3472621;

Automatic exact mappings (from CISMeF team)
- Myeloid neoplasms with PDGFRB rearrangement [ICD-11 Extension code]
Currated CISMeF NLP mapping
- Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement (morphologic abnormality) [SNOMED CT concept]
- Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement [ORDO Disease]
- myeloid and lymphoid neoplasms associated with PDGFRB rearrangement [DO Concept]
DO Cross reference
- myeloid and lymphoid neoplasms associated with PDGFRB rearrangement [DO Concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Myeloid neoplasm associated with beta-type platelet-derived growth factor receptor gene rearrangement (disorder) [SNOMED CT concept]
- Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement (morphologic abnormality) [SNOMED CT concept]
- Myeloid-lymphoid neoplasm with PDGFRB rearrangement (morphologic abnormality) [SNOMED CT concept]
- Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement [ORDO Disease]
- myeloid and lymphoid neoplasms associated with PDGFRB rearrangement [DO Concept]
concept_is_in_subset
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- NCIt Neoplasm Core 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
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_molecular_abnormality
- 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
- PDGFRB Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- PDGFRB Gene [NCIt concept]
- PDGFRB wt Allele [NCIt concept]

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