B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1

Preferred Label : B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1;

NCIt synonyms : B-Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34;q11.2); BCR-ABL1; B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34;q11.2); BCR-ABL1; B Lymphoblastic Leukemia Lymphoma with t 9 22 q34 q11 2 BCR-ABL 1; B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34.1;q11.2); BCR::ABL1; B Lymphoblastic Leukemia/Lymphoma with BCR-ABL1 Fusion; B Lymphoblastic Leukemia/Lymphoma with BCR::ABL1 Fusion; B-Lymphoblastic Leukemia/Lymphoma with BCR-ABL1 Fusion; B-Lymphoblastic Leukemia/Lymphoma with BCR::ABL1 Fusion;

NCIt definition : A precursor lymphoid neoplasm which is composed of B-lymphoblasts and carries a translocation between the BCR gene on chromosome 22 and the ABL1 gene on chromosome 9. It results in the production of the p190 kd or p210 kd fusion protein. It has an unfavorable clinical outcome.;

Neoplastic status : Malignant;

ICD-O code : 9812/3;

Details

Origin ID

C80331;

UMLS CUI

C2698317;

Automatic exact mappings (from CISMeF team)
- B lymphoblastic leukemia lymphoma with t(9;22)(q34;q11.2); BCR-ABL1 (morphologic abnormality) [SNOMED CT concept]
DO Cross reference
- B-lymphoblastic leukemia/lymphoma with BCR-ABL1 [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
- Hepatomegaly [NCIt concept]
- Lymphadenopathy [NCIt concept]
- Unfavorable Clinical Outcome [NCIt concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- B lymphoblastic leukemia lymphoma with t(9;22)(q34;q11.2); BCR-ABL1 (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_mapped_to_gene
- ABL1 Gene [NCIt concept]
- BCR/ABL1 Fusion Gene [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]
pathogenesis_of_disease_involves_gene
- ABL1 Gene [NCIt concept]
- ABL1 wt Allele [NCIt concept]
- BCR/ABL1 Fusion Gene [NCIt concept]
- BCR/ABL1 Fusion Gene p190 [NCIt concept]
- BCR/ABL1 Fusion Gene p210 [NCIt concept]
- BCR/ABL1 Fusion Gene p230 [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.1052T>C Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.1075T>G Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.1150C>A Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.1187A>C Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.1187A>G Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.1457T>C Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.742C>G Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.749G>A Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.756G>C Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.756G>T Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.758A>T Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.763G>A Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.764A>T Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.827A>G Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.835G>A Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.895G>C Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.895G>T Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.944C>T Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.949T>C Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.951C>A Mutation [NCIt concept]
- BCR/ABL1 Fusion Gene with ABL1 NM_005157.4:c.951C>G Mutation [NCIt concept]

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