Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA

Preferred Label : Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA;

NCIt synonyms : Childhood Acute Promyelocytic Leukemia; Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML::RARA; Childhood Acute Promyelocytic Leukemia with PML-RARA; Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML::RARA Fusion; Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA Fusion;

NCIt related terms : Acute Promyelocytic Leukemia with PML-RARA; Childhood APL with t(15;17)(q24.1;q21.2); PML-RARA; APL with PML-RARA; Childhood APML with t(15;17)(q24.1;q21.2); PML-RARA;

NCIt definition : An acute promyelocytic leukemia with t(15;17)(q24.1;q21.2); PML-RARA that occurs in children.;

Neoplastic status : Malignant;

Détails

Origin ID

C7968;

UMLS CUI

C0279641;

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]
- 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]
- RARA Gene Rearrangement [NCIt concept]
- t(15;17)(q24;q21) [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Disease Characteristics Table [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP 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]
- Neoplastic Promyelocyte [NCIt concept]
disease_has_accepted_treatment_with_regimen
- CCG-0922 APL Regimen [NCIt concept]
- COG-C9710 APL Regimen [NCIt concept]
- IDA-FLAG Regimen [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]
- Neoplastic Promyelocytes in Bone Marrow Markedly Increased [NCIt concept]
- Recurrent Genetic Abnormalities Present [NCIt concept]
disease_has_molecular_abnormality
- Fusion Protein Expression [NCIt concept]
- PML-RARA 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
- PML/RARA 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]

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