Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A

Preferred Label : Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A;

NCIt synonyms : Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3 (AF9)-KMT2A; Acute Myeloid Leukemia with t 9 11 p22 q23 MLLT3-MLL; Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-MLL; Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3::KMT2A; Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3::MLL; Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A Fusion; Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3::KMT2A Fusion;

NCIt related terms : Acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL; AML with t(9;11)(p22;q33);MLLT3-MLL; AML with t(9;11)(p21.3;q23.3); KMT2A-MLLT3;

NCIt definition : An acute myeloid leukemia associated with t(9;11)(p21.3;q23.3) and MLLT3-KMT2A fusion protein expression. Morphologically it usually has monocytic features. It may present at any age but it is more commonly seen in children. Patients may present with disseminated intravascular coagulation.;

Neoplastic status : Malignant;

ICD-O code : 9897/3;

Détails

Origin ID

C82403;

UMLS CUI

C2919692;

Automatic exact mappings (from CISMeF team)
- Acute myeloid leukemia with 11q23-abnormality [ICD-10 Sub-category]
Currated CISMeF NLP mapping
- Acute myeloid leukemia with KMT2A rearrangement (morphologic abnormality) [SNOMED CT concept]
- Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL (disorder) [SNOMED CT concept]
- Acute myeloid leukemia, 11q23 abnormalities [ICD-O code]
- acute myeloid leukemia with 11q23 abnormalities [Disease (Nov.)]
Disease excludes abnormal cell
- Neoplastic Lymphoblast [NCIt concept]
Disease excludes normal cell origin
- Lymphocyte [NCIt concept]
Disease may have findings
- Disseminated Intravascular Coagulation [NCIt concept]
- Hypercellular Bone Marrow [NCIt concept]
Has associated anatomic sites
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
Has cytogenetic abnormalities
- Chromosomal Rearrangement [NCIt concept]
- MLLT3 Gene Rearrangement [NCIt concept]
See also inter- (CISMeF)
- Acute myeloid leukemia with 11q23 abnormalities [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL (disorder) [SNOMED CT concept]
- Acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL (morphologic abnormality) [Inactive SNOMED CT concept]
- acute myeloid leukemia with 11q23 abnormalities [Disease (Nov.)]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Disease Characteristics Table [NCIt concept]
- CPTAC Acute Myeloid Leukemia Baseline Form [NCIt concept]
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Codelists Terminology [NCIt concept]
- CPTAC Neoplasms Codelist [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [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]
- 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]
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]
- KMT2A/MLLT3 Fusion Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- KMT2A/MLLT3 Fusion Gene [NCIt concept]

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