Status: current, Defined. Date: 30-Sep 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5098014011 | Acute myeloid leukemia with BCR-ABL1 | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5098015012 | Acute myeloid leukemia with BCR-ABL1 (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
5098016013 | Acute myeloid leukemia with t(9;22)(q34.1;q11.2) | en | Synonym | Active | Case insensitive | SNOMED CT core |
5098017016 | Acute myeloid leukaemia with BCR-ABL1 | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5098018014 | Acute myeloid leukaemia with t(9;22)(q34.1;q11.2) | en | Synonym | Active | Case insensitive | SNOMED CT core |
5098019018 | A rare acute myeloid leukemia (AML) with recurrent genetic anomaly characterized by the presence of bone marrow and peripheral blood myeloblasts with features ranging from those of minimal differentiation to granulocytic maturation, demonstrating t(9;22)(q34.1;q11.2) or molecular genetic evidence of BCR-ABL1 fusion. Evidence of chronic myeloid leukemia (CML) is absent. Patients most commonly present with leukocytosis with blast predominance and variable anemia and thrombocytopenia. Splenomegaly is less frequent and peripheral blood basophilia lower than in patients with myeloid blast transformation of CML. The disease occurs primarily in adults, and response to traditional AML therapy or tyrosine kinase inhibitor therapy alone is typically poor. | en | Definition | Active | Case sensitive | SNOMED CT core |
5098020012 | A rare acute myeloid leukaemia (AML) with recurrent genetic anomaly characterised by the presence of bone marrow and peripheral blood myeloblasts with features ranging from those of minimal differentiation to granulocytic maturation, demonstrating t(9;22)(q34.1;q11.2) or molecular genetic evidence of BCR-ABL1 fusion. Evidence of chronic myeloid leukaemia (CML) is absent. Patients most commonly present with leucocytosis with blast predominance and variable anaemia and thrombocytopenia. Splenomegaly is less frequent and peripheral blood basophilia lower than in patients with myeloid blast transformation of CML. The disease occurs primarily in adults, and response to traditional AML therapy or tyrosine kinase inhibitor therapy alone is typically poor. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Acute myeloid leukaemia with BCR-ABL1 | Is a | Acute myeloid leukaemia due to recurrent genetic abnormality | true | Inferred relationship | Some | ||
Acute myeloid leukaemia with BCR-ABL1 | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 | |
Acute myeloid leukaemia with BCR-ABL1 | Associated morphology | Acute myeloid leukaemia with BCR-ABL1 | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set