Status: current, Defined. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3655684018 | Inherited acute myeloid leukemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3655685017 | Inherited acute myeloid leukaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3655686016 | Inherited acute myeloid leukemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3655687013 | Pure familial acute myeloid leukemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3655688015 | Pure familial acute myeloid leukaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3655689011 | A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis) and genetic defects predisposing to acute myeloid leukemia. Patients present with signs and symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 3655690019 | A rare malignant haematologic disease characterised by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis) and genetic defects predisposing to acute myeloid leukaemia. Patients present with signs and symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited acute myeloid leukaemia | Associated morphology | Acute myeloid leukaemia | true | Inferred relationship | Some | 1 | |
| Inherited acute myeloid leukaemia | Associated with | Congenital disease | true | Inferred relationship | Some | 2 | |
| Inherited acute myeloid leukaemia | Is a | Acute myeloid leukemia, disease | true | Inferred relationship | Some | ||
| Inherited acute myeloid leukaemia | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Inherited acute myeloid leukaemia | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 | |
| Inherited acute myeloid leukaemia | Associated morphology | Acute myeloid leukaemia - category | false | 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
Description inactivation indicator reference set
FHIR