Preferred Label : Chronic Myeloid Leukemia, Philadelphia Chromosome Positive, BCR-ABL1 Positive;
NCIt synonyms : Ph' Positive Chronic Granulocytic Leukemia; Philadelphia Chromosome Positive Chronic Myelogenous Leukemia; Ph' Chromosome Positive Chronic Myelocytic Leukemia; Ph1 Chromosome Positive Chronic Myelogenous Leukemia; Chronic Myeloid Leukemia t(9;22) (q34;q11), BCR/ABL Positive; Ph1 Chromosome Positive Chronic Myeloid Leukemia; Ph1 Positive Chronic Granulocytic Leukemia; Philadelphia Chromosome Positive Chronic Myeloid Leukemia; Ph' Chromosome Positive Chronic Myelogenous Leukemia; Ph' Chromosome Positive Chronic Myeloid Leukemia; Ph1 Chromosome Positive Chronic Myelocytic Leukemia; Philadelphia Chromosome Positive CML; Philadelphia Chromosome Positive Chronic Granulocytic Leukemia; Philadelphia Chromosome Positive Chronic Myelocytic Leukemia; Philadelphia Chromosome Positive, BCR::ABL1 Positive Chronic Myelogenous Leukemia; Chronic Myeloid Leukemia, Philadelphia Chromosome Positive, BCR::ABL1 Positive;
NCIt related terms : Chronic granulocytic leukemia, t(9;22)(q34;q11); Chronic myelogenous leukemia, Philadelphia chromosome (Ph 1) positive; Chronic myelogenous leukemia, Philadelphia chromosome positive; CML - Philadelphia chromosome; Chronic granulocytic leukemia, Philadelphia chromosome (Ph1) positive; Chronic myelogenous leukemia, t(9;22)(q34;q11); Chronic granulocytic leukemia, BCR/ABL; Philadelphia Chromosome Positive, BCR-ABL1 Positive Chronic Myelogenous Leukemia;
NCIt definition : A chronic myeloid leukemia characterised by the t(9;22)(q34;q11) chromosomal translocation,
resulting in the presence of the Philadelphia chromosome and the BCR-ABL1 fusion gene.;
Neoplastic status : Malignant;
Codes from synonyms : 10009013;
Origin ID : C9128;
UMLS CUI : C0279543;
- Automatic exact mappings (from CISMeF team)
- Disease excludes normal cell origin
- Disease may have findings
- Has associated anatomic sites
- Has cytogenetic abnormalities
- Semantic type(s)
- UMLS correspondences (same concept)
- Validated automatic mappings to NTBT
- concept_is_in_subset
- disease_excludes_finding
- disease_excludes_molecular_abnormality
- disease_has_abnormal_cell
- disease_has_finding
- disease_has_molecular_abnormality
- disease_has_normal_cell_origin
- disease_has_normal_tissue_origin
- disease_has_primary_anatomic_site
- disease_mapped_to_gene
- disease_may_have_associated_disease
- disease_may_have_molecular_abnormality