Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3655685017 | Inherited acute myeloid leukaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3655686016 | Inherited acute myeloid leukemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3655687013 | Pure familial acute myeloid leukemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3655688015 | Pure familial acute myeloid leukaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited acute myeloid leukemia (disorder) | Associated with | Congenital disease (disorder) | true | Inferred relationship | Some | 2 | |
| Inherited acute myeloid leukemia (disorder) | Is a | Acute myeloid leukemia, disease | true | Inferred relationship | Some | ||
| Inherited acute myeloid leukemia (disorder) | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Inherited acute myeloid leukemia (disorder) | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 | |
| Inherited acute myeloid leukemia (disorder) | Associated morphology | Acute myeloid leukemia - category | false | Inferred relationship | Some | 1 | |
| Inherited acute myeloid leukemia (disorder) | Associated morphology | Acute myeloid leukemia (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
FHIR