Preferred Label : Acute Lymphoblastic Leukemia;
NCIt synonyms : Precursor Lymphoblastic Leukemia; Lymphoblastic Leukemia; Precursor Cell Lymphoblastic Leukemia; ALL - Acute Lymphocytic Leukemia; Acute Lymphocytic Leukemias; Acute Lymphocytic Leukaemia; Acute Lymphogenous Leukemia;
NCIt related terms : LEUKEMIA, LYMPHOBLASTIC, MALIGNANT; Precursor cell lymphoblastic leukemia, NOS; Acute Lymphocytic Leukemia; Acute lymphoblastic leukemia, NOS; Acute lymphoblastic leukemia, precursor cell type; Acute lymphatic leukemia; Precursor Lymphoblasic Leukemia; Acute lymphoblastic leukemia (ALL); Lymphoblastic leukemia, NOS; ALL_TYPE; ALL; Acute lymphoid leukemia;
NCIt definition : Leukemia with an acute onset, characterized by the presence of lymphoblasts in the
bone marrow and the peripheral blood. It includes the acute B lymphoblastic leukemia
and acute T lymphoblastic leukemia.;
Alternative definition : NICHD: A rapidly progressive cancer of the blood and bone marrow consisting of the
proliferation of lymphoblasts, which are immature, dysfunctional white blood cells.; CDISC: A progressive, proliferative disease of blood cells, originating from immature
lymphoid cells.; NCI-GLOSS: An aggressive (fast-growing) type of leukemia (blood cancer) in which too
many lymphoblasts (immature white blood cells) are found in the blood and bone marrow.;
Neoplastic status : Malignant;
ICD-O code : 9835/3;
Codes from synonyms : CDR0000044362; 10000846; CDR0000046332; CDR0000045586;
Origin ID : C3167;
UMLS CUI : C0023449;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
DO Cross reference
Disease excludes abnormal cell
Disease excludes normal cell origin
Disease may have findings
False automatic mappings
Has associated anatomic sites
Semantic type(s)
UMLS correspondences (same concept)
associated_with_malfunction_of_gene_product
concept_is_in_subset
disease_excludes_finding
disease_has_abnormal_cell
disease_has_associated_gene
disease_has_finding
disease_has_normal_cell_origin
disease_has_normal_tissue_origin
disease_has_primary_anatomic_site
disease_may_have_molecular_abnormality
may_be_associated_disease_of_disease