| acute myeloïde leukemie met BCR-ABL1 (aandoening) | | acute myeloïde leukemie met BCR-ABL1 | | acute myeloblastenleukemie met BCR-ABL1
BCR-ABL1-positieve AML
| | Acute myeloid leukemia with BCR-ABL1 | | Acute myeloid leukemia with t(9;22)(q34.1;q11.2)
| | 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. |
| | Id | 1237368006 | | Status | Defined |
| SNOMED CT to Orphanet simple map | 585867 |
| SNOMED CT to ICD-10 extended map | | Target | C92.7 | | Rule | TRUE | | Advice | ALWAYS C92.7 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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