Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement

Preferred Label : Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement;

NCIt synonyms : 8p11 Myeloproliferative Syndrome; 8p11 Stem Cell Leukemia/Lymphoma Syndrome; 8p11 Stem Cell Lymphoma/Leukemia Syndrome; 8p11 Stem Cell Syndrome; Myeloid and Lymphoid Neoplasms with FGFR1 Rearrangement; M/LN-eo with FGFR1 Rearrangement; Myeloid/Lymphoid Neoplasm with FGFR1 Rearrangement;

NCIt related terms : Myeloid and lymphoid neoplasms with FGFR1 abnormalities;

NCIt definition : Hematologic neoplasms characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint. Patients present with a myeloproliferative neoplasm, acute myeloid leukemia, lymphoblastic lymphoma/leukemia of T or B-cell lineage, or acute leukemia of mixed phenotype.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL497893;

ICD-O code : 9967/3;

Details

Origin ID

C84277;

UMLS CUI

C3150773;

Automatic exact mappings (from CISMeF team)
- Myeloid and lymphoid neoplasm with fibroblast growth factor receptor 1 abnormality (disorder) [SNOMED CT concept]
- Myeloid and lymphoid neoplasms with FGFR1 abnormalities [ICD-11 Extension code]
- Myeloid or lymphoid neoplasms with FGFR1 abnormalities [ICD-11 Category]
- Myeloid-lymphoid neoplasm with FGFR1 rearrangement (morphologic abnormality) [SNOMED CT concept]
Currated CISMeF NLP mapping
- 8p11 myeloproliferative syndrome [Disease (Nov.)]
- Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement [ORDO Disease]
DO Cross reference
- myeloid and lymphoid neoplasms associated with FGFR1 abnormalities [DO Concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- 8p11 myeloproliferative syndrome [Disease (Nov.)]
- Chromosome 8p11 myeloproliferative syndrome [OMIM Phenotype]
- Myeloid and lymphoid neoplasm with fibroblast growth factor receptor 1 abnormality (disorder) [SNOMED CT concept]
- Myeloid-lymphoid neoplasm with FGFR1 rearrangement (morphologic abnormality) [SNOMED CT concept]
- Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement [ORDO Disease]
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]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 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
- FGFR1 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
- BCR/FGFR1 Fusion Gene [NCIt concept]
- FGFR1 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- BCR-FGFR1 Fusion Protein Expression [NCIt concept]
pathogenesis_of_disease_involves_gene
- BCR/FGFR1 Fusion Gene [NCIt concept]
- FGFR1 Gene [NCIt concept]
- FGFR1 wt Allele [NCIt concept]

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