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FHIR
© HL7.org
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Server Home |
FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR Version n/a
User: [n/a]
Status: current, Not 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 |
| 3441962012 | Acute myeloid leukemia with t(8;16)(p11;p13) translocation (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3441963019 | 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 |
| 3441964013 | 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 |
| 5134571013 | Acute myeloid leukemia with KAT6A::CREBBP fusion | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5134572018 | Acute myeloid leukaemia with KAT6A::CREBBP fusion | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (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 (morphologic abnormality) | Is a | Acute myeloid leukemia with recurrent genetic abnormality | false | Inferred relationship | Some | ||
| Acute myeloid leukemia with t(8;16)(p11;p13) translocation (morphologic abnormality) | Is a | Acute myeloid leukemia (morphologic abnormality) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| A distinct form of acute myeloid leukemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and 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. | Associated morphology | True | Acute myeloid leukemia with t(8;16)(p11;p13) translocation (morphologic abnormality) | Inferred relationship | Some | 1 |
This concept is not in any reference sets