Hyperdiploid B Lymphoblastic Leukemia/Lymphoma

Preferred Label : Hyperdiploid B Lymphoblastic Leukemia/Lymphoma;

NCIt synonyms : B-Lymphoblastic Leukemia/Lymphoma with Hyperdiploidy; B Lymphoblastic Leukemia Lymphoma with Hyperdiploidy; B Lymphoblastic Leukemia/Lymphoma with High Hyperdiploidy; B-Lymphoblastic Leukemia/Lymphoma with High Hyperdiploidy;

NCIt related terms : High Hyperdiploidy; B lymphoblastic leukemia/lymphoma with hyperdiploidy;

NCIt definition : A precursor lymphoid neoplasm composed of B lymphoblasts which contain more than 50 and usually less than 66 chromosomes. It has a favorable clinical outcome.;

Neoplastic status : Malignant;

ICD-O code : 9815/3;

Details

Origin ID

C80335;

UMLS CUI

C2698311;

Automatic exact mappings (from CISMeF team)
- B lymphoblastic leukemia lymphoma with hyperdiploidy (disorder) [SNOMED CT concept]
CISMeF manual mappings
- B lymphoblastic leukemia lymphoma with hyperdiploidy (morphologic abnormality) [SNOMED CT concept]
Currated CISMeF NLP mapping
- B lymphoblastic leukaemia/lymphoma with hyperdiploidy [ICD-11 Extension code]
- B-lymphoblastic leukemia/lymphoma with hyperdiploidy [DO Concept]
- B-lymphoblastic leukemia/lymphoma with hyperdiploidy [ORDO Disease]
DO Cross reference
- B-lymphoblastic leukemia/lymphoma with hyperdiploidy [DO Concept]
Disease excludes abnormal cell
- Neoplastic T-Lymphocyte and Neoplastic Natural Killer Cell [NCIt concept]
Disease excludes normal cell origin
- Mature B-Lymphocyte [NCIt concept]
- Myeloid Cell [NCIt concept]
Disease may have findings
- Favorable Clinical Outcome [NCIt concept]
- Hepatomegaly [NCIt concept]
- Lymphadenopathy [NCIt concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Has cytogenetic abnormalities
- Hyperdiploidy [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- B lymphoblastic leukemia lymphoma with hyperdiploidy (disorder) [SNOMED CT concept]
- B lymphoblastic leukemia lymphoma with hyperdiploidy (morphologic abnormality) [SNOMED CT 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]
- 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_has_abnormal_cell
- Abnormal Lymphocyte [NCIt concept]
- Malignant Cell [NCIt concept]
- Neoplastic B-Lymphoblast [NCIt concept]
- Neoplastic B-Lymphocyte [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Hematopoietic and Lymphoid Cell [NCIt concept]
- Neoplastic Lymphoblast [NCIt concept]
- Neoplastic Lymphocyte [NCIt concept]
disease_has_finding
- Malignant Cellular Infiltrate [NCIt concept]
- Recurrent Genetic Abnormalities Present [NCIt concept]
disease_has_molecular_abnormality
- Clonal Immunoglobulin Gene Rearrangement [NCIt concept]
disease_has_normal_cell_origin
- B-Lymphocyte [NCIt concept]
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Lymphoblast [NCIt concept]
- Lymphocyte [NCIt concept]
- Precursor B-Lymphoblast [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
- Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]
- Lymphatic System [NCIt concept]
disease_may_have_molecular_abnormality
- Clonal Immunoglobulin Heavy Chain Gene Rearrangement [NCIt concept]
- Clonal Immunoglobulin Kappa Light Chain Gene Rearrangement [NCIt concept]
- Clonal T-Cell Receptor Beta Chain Gene Rearrangement [NCIt concept]
- Clonal T-Cell Receptor Gamma Chain Gene Rearrangement [NCIt concept]

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