Childhood Chronic Myeloid Leukemia, BCR-ABL1 Positive

Preferred Label : Childhood Chronic Myeloid Leukemia, BCR-ABL1 Positive;

NCIt synonyms : Childhood Chronic Myelogenous Leukemia; Childhood Chronic Myeloid Leukemia; Childhood CML; Childhood Chronic Myelogenous Leukemia, BCR::ABL1 Positive; Childhood Chronic Myeloid Leukemia, BCR::ABL1 Positive; Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive;

NCIt related terms : Chronic Myelogenous Leukemia (CML);

NCIt definition : A chronic myeloid leukemia, BCR-ABL1 positive occurring during childhood.;

Alternative definition : NICHD: A BCR-ABL1 positive chronic myelogenous leukemia occurring during childhood.;

Neoplastic status : Malignant;

Details

Origin ID

C7320;

UMLS CUI

C1327920;

Automatic exact mappings (from CISMeF team)
- chronic myeloid leukemia [DO Concept]
- leukemia, myelogenous, chronic, bcr-abl positive [MeSH Descriptor]
Disease excludes normal cell origin
- Lymphocyte [NCIt concept]
Disease may have findings
- Chronic Clinical Course [NCIt concept]
- Fatigue [NCIt concept]
- Hepatomegaly [NCIt concept]
- Leukocytosis [NCIt concept]
- Weight Loss [NCIt concept]
Has associated anatomic sites
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
Validated automatic mappings to NTBT
- Chronic myeloid leukemia [ORDO Disease]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Ineffective Hematopoiesis [NCIt concept]
- Solid Growth Pattern [NCIt concept]
disease_excludes_molecular_abnormality
- FGFR1 Gene Rearrangement [NCIt concept]
- PDGFRA Gene Rearrangement [NCIt concept]
- PDGFRB Gene Rearrangement [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 Myeloid Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Hypercellular Bone Marrow [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Splenomegaly [NCIt concept]
disease_has_molecular_abnormality
- BCR-ABL1 Fusion Protein Expression [NCIt concept]
disease_has_normal_cell_origin
- Bone Marrow Stem Cell [NCIt concept]
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Pluripotent 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
- ABL1 Gene [NCIt concept]
- BCR/ABL1 Fusion Gene [NCIt concept]
disease_may_have_associated_disease
- Anemia [NCIt concept]
may_be_associated_disease_of_disease
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas [NCIt concept]
- Recurrent Neurofibromatosis Type 1 [NCIt concept]
- Refractory Neurofibromatosis Type 1 [NCIt concept]

Keyword's position in hierarchy(ies) :

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