Status: current, Defined. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3644020014 | Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3644021013 | Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3644022018 | Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3644023011 | A rare subtype of acute myeloid leukemia with recurrent cytogenetic abnormalities characterized by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anemia, thrombocytopenia and nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 3644024017 | A rare subtype of acute myeloid leukaemia with recurrent cytogenetic abnormalities characterised by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anaemia, thrombocytopenia and nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | Is a | Acute myeloid leukaemia due to recurrent genetic abnormality | true | Inferred relationship | Some | ||
| Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | Associated morphology | Acute myeloid leukaemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1 | true | Inferred relationship | Some | 1 | |
| Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set
FHIR