Acute Promyelocytic Leukemia with t(5;17)(q35;q21); NPM1-RARA

Preferred Label : Acute Promyelocytic Leukemia with t(5;17)(q35;q21); NPM1-RARA;

NCIt synonyms : Acute Promyelocytic Leukemia with t 5 17 q32 q12; Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1::RARA; Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1-RARA Fusion; Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1::RARA Fusion; Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1-RARA; Acute Promyelocytic Leukemia with t(5;17)(q35;q21); NPM1::RARA;

NCIt related terms : AML with t(5;17)(q35;q21); AML with t(5;17)(q35;q21);NPM1-RARA; Acute Myeloid Leukemia with t(5;17)(q35;q21);NPM1-RARA; Acute Myeloid Leukemia with t(5;17)(q35;q21);

NCIt definition : Acute promyelocytic leukemia with a variant RARA rearrangement associated with t(5;17)(q35;q21) that results in the expression of NPM1-RARA fusion protein.;

Alternative definition : NICHD: An acute myeloid leukemia associated with t(5;17)(q35;q21) and NPM1-RARA fusion protein expression. This type of leukemia often has the morphologic features of acute promyelocytic leukemia. There have been rare cases in children reported in the literature.;

Neoplastic status : Malignant;

Details

Origin ID

C36057;

UMLS CUI

C4055494;

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]
Has associated anatomic sites
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
Has cytogenetic abnormalities
- Chromosomal Rearrangement [NCIt concept]
- RARA Gene Rearrangement [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- NCIt Neoplasm Core Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_excludes_cytogenetic_abnormality
- t(15;17)(q24;q21) [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_excludes_molecular_abnormality
- PML-RARA Fusion Protein Expression [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]
- Neoplastic Promyelocyte [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]
- Neoplastic Promyelocytes in Bone Marrow Markedly Increased [NCIt concept]
- Recurrent Genetic Abnormalities Present [NCIt concept]
disease_has_molecular_abnormality
- Fusion Protein Expression [NCIt concept]
disease_has_normal_cell_origin
- Bone Marrow Stem Cell [NCIt concept]
- Bone Marrow Stem Cell with Potential to Differentiate to Granulocytic Lineage [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
- NPM1/RARA Long Fusion Gene [NCIt concept]
- NPM1/RARA Short Fusion Gene [NCIt concept]
- RARA Gene [NCIt concept]
disease_may_have_abnormal_cell
- Faggot Cell [NCIt concept]
disease_may_have_associated_disease
- Disseminated Intravascular Coagulation [NCIt concept]
pathogenesis_of_disease_involves_gene
- NPM1/RARA Long Fusion Gene [NCIt concept]
- NPM1/RARA Short Fusion Gene [NCIt concept]

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