Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-KMT2A

Preferred Label : Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-KMT2A;

NCIt synonyms : Acute Myeloid Leukemia (AML) with t(10;11)(p12.3;q23.3); KMT2A::MLLT10; Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLL-MLLT10; Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-MLL; Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10::KMT2A Fusion; Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-KMT2A Fusion;

NCIt related terms : Acute Myeloid Leukemia (AML) with t(10;11)(p12.3;q23.3); MLL-MLLT10;

NCIt definition : An acute myeloid leukemia characterized by t(10;11)(p12.3;q23.3) resulting in MLLT10-KMT2A gene fusion. It is associated with an unfavorable prognosis.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL521169;

Details

Origin ID

C132101;

UMLS CUI

C4329272;

Disease excludes abnormal cell
- Neoplastic Lymphoblast [NCIt concept]
Disease excludes normal cell origin
- Lymphocyte [NCIt concept]
Disease may have findings
- Hypercellular Bone Marrow [NCIt concept]
- Unfavorable Clinical Outcome [NCIt concept]
Has associated anatomic sites
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
Has cytogenetic abnormalities
- Chromosomal Rearrangement [NCIt concept]
- t(10;11)(p12;q23) [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_cytogenetic_abnormality
- MLLT3 Gene Rearrangement [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Chronic Clinical Course [NCIt concept]
- Cytogenetic Abnormalities Not Detected [NCIt concept]
- Solid Growth Pattern [NCIt concept]
disease_has_abnormal_cell
- Leukemic Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Hematopoietic and Lymphoid Cell [NCIt concept]
- Neoplastic Myeloblast [NCIt concept]
- Neoplastic Myeloid Cell [NCIt concept]
disease_has_finding
- Blasts 10 Percent or More of Bone Marrow Nucleated Cells [NCIt concept]
- Blasts 10 Percent or More of Peripheral Blood White Cells [NCIt concept]
- Childhood Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Recurrent Genetic Abnormalities Present [NCIt concept]
disease_has_molecular_abnormality
- Fusion Protein Expression [NCIt concept]
- KMT2A Gene Rearrangement [NCIt concept]
- KMT2A-MLLT10 Fusion Protein Expression [NCIt concept]
disease_has_normal_cell_origin
- Bone Marrow Stem Cell [NCIt concept]
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Multipotent Bone Marrow Stem Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic Tissue [NCIt concept]
- 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
- KMT2A Gene [NCIt concept]
- MLL/MLLT10 Fusion Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- MLL/MLLT10 Fusion Gene [NCIt concept]

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