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 characterized 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