Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3441957011 | Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3441958018 | Acute myeloid leukemia with t(8;16)(p11;p13) translocation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3441959014 | Acute myeloid leukaemia with t(8;16)(p11;p13) translocation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 760991000241112 | leucémie myéloblastique aigüe associée à une translocation t(8;16)(p11;p13) (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 989541000172117 | leucémie myéloblastique aigüe associée à une translocation t(8;16)(p11;p13) | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3441960016 | A distinct form of acute myeloid leukemia in which this chromosomal anomaly is found de novo or in therapy-related cases. The disease is characterized by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3441961017 | A distinct form of acute myeloid leukaemia in which this chromosomal anomaly is found de novo or in therapy-related cases. The disease is characterised by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) | est un(e) (attribut) | Acute myeloid leukemia due to recurrent genetic abnormality (disorder) | true | Inferred relationship | Some | ||
| Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) | morphologie associée (attribut) | Acute myeloid leukemia with t(8;16)(p11;p13) translocation (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) | localisation d'une constatation (attribut) | Bone marrow structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR