Acute Myeloid Leukemia with CEBPA Mutation

Preferred Label : Acute Myeloid Leukemia with CEBPA Mutation;

NCIt synonyms : Non-Familial Acute Myeloid Leukemia with Mutated CEBPA; Acute Myeloid Leukemia with Non-Germline Mutated CEBPA;

NCIt related terms : AML with Mutated CEBPA; Acute Myeloid Leukemia with Mutated CEBPA;

NCIt definition : An acute myeloid leukemia with non-germline mutations of the CEBPA gene.;

Alternative definition : NICHD: An acute myeloid leukemia (AML) with mutation of the CEBPA gene. It is usually associated with normal karyotype, and most cases meet the criteria for AML with or without maturation.;

Neoplastic status : Malignant;

ICD-O code : 9861/3;

Details

Origin ID

C82433;

UMLS CUI

C4707178;

Currated CISMeF NLP mapping
- Acute myeloid leukaemia with mutated CEBPA [ICD-11 Extension code]
- Acute myeloid leukemia with CEBPA mutation (morphologic abnormality) [SNOMED CT concept]
Disease excludes abnormal cell
- Neoplastic Lymphoblast [NCIt concept]
Disease excludes normal cell origin
- Lymphocyte [NCIt concept]
Disease may have findings
- Favorable Clinical Outcome [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]
See also inter- (CISMeF)
- Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) [SNOMED CT concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) [SNOMED CT concept]
- Acute myeloid leukemia with CEBPA mutation (morphologic abnormality) [SNOMED CT concept]
Validated automatic mappings to BTNT
- Acute myeloid leukemia with biallelic mutation of CEBPA [ICD-11 Extension code]
associated_with_malfunction_of_gene_product
- CCAAT/Enhancer Binding Protein Alpha [NCIt concept]
concept_is_in_subset
- CPTAC Acute Myeloid Leukemia Baseline Form [NCIt concept]
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC 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]
- Hereditary Lesion [NCIt concept]
- Recurrent Genetic Abnormalities Present [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
- CEBPA Gene Mutation [NCIt concept]
- Fusion Protein Expression [NCIt concept]
disease_has_normal_cell_origin
- Bone Marrow Stem Cell [NCIt concept]
- Hematopoietic and Lymphoid 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
- CEBPA Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- CEBPA Gene [NCIt concept]
- CEBPA wt Allele [NCIt concept]

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