Mixed Phenotype Acute Leukemia with BCR-ABL1 Fusion

Preferred Label : Mixed Phenotype Acute Leukemia with BCR-ABL1 Fusion;

NCIt synonyms : Mixed Phenotype Acute Leukemia with t 9 22 q34 q11 2 BCR-ABL1; Mixed Phenotype Acute Leukemia with t(9;22)(q34.1;q11.2); BCR::ABL1; MPAL with t(9;22)(q34.1;q11.2); BCR-ABL1; MPAL with t(9;22)(q34.1;q11.2); BCR::ABL1; Mixed Phenotype Acute Leukemia with BCR::ABL1 Fusion; Mixed-Phenotype Acute Leukemia with BCR::ABL1 Fusion; Mixed-Phenotype Acute Leukemia with BCR-ABL1 Fusion;

NCIt related terms : Mixed phenotype acute leukemia with t(9;22)(q34;q11.2); BCR-ABL1; Mixed Phenotype Acute Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1;

NCIt definition : A rare mixed phenotype acute leukemia in which the blasts carry the chromosomal translocation t(9;22)(q34.1;q11.2) that results in BCR-ABL1 gene fusion. The prognosis is usually unfavorable.;

Neoplastic status : Malignant;

ICD-O code : 9806/3;

Details

Origin ID

C82192;

UMLS CUI

C2826037;

Currated CISMeF NLP mapping
- Mixed phenotype acute leukaemia with t(9;22) (q34;q11.2); BCR-ABL1 [ICD-11 More detail]
- Mixed phenotype acute leukemia with t(9;22) (q34;q11.2); BCR-ABL1 (disorder) [SNOMED CT concept]
- Mixed phenotype acute leukemia with t(9;22)(q34;q11.2); BCR-ABL1 (morphologic abnormality) [SNOMED CT concept]
Disease may have findings
- Granulocytopenia [NCIt concept]
- Ineffective Hematopoiesis [NCIt concept]
- Thrombocytopenia [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)
- Mixed phenotype acute leukaemia with t(9;22) (q34;q11.2); BCR-ABL1 [ICD-11 More detail]
- Mixed phenotype acute leukemia with t(9;22) (q34;q11.2); BCR-ABL1 (disorder) [SNOMED CT concept]
- Mixed phenotype acute leukemia with t(9;22)(q34;q11.2); BCR-ABL1 (morphologic abnormality) [SNOMED CT concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- 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]
- Blasts Expressing CD56 and Immature T-Cell Markers Present [NCIt concept]
- Chronic Clinical Course [NCIt concept]
- Solid Growth Pattern [NCIt concept]
disease_has_abnormal_cell
- Leukemic Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Neoplastic Blast [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_finding
- Blasts of Mixed Phenotype Present [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Recurrent Genetic Abnormalities Present [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Multipotent Bone Marrow Stem Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
disease_mapped_to_gene
- ABL1 Gene [NCIt concept]
- BCR/ABL1 Fusion Gene [NCIt concept]
disease_may_have_associated_disease
- Anemia [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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