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 |
| 3655314019 | Acute myeloid leukaemia with CEBPA somatic mutations | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3655316017 | Acute myeloid leukemia with CEBPA somatic mutations | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3655317014 | Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3655318016 | Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3655319012 | Acute myeloid leukaemia with CCAAT/enhancer binding protein alpha somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5404390015 | A subtype of acute myeloid leukemia with recurrent genetic abnormalities, characterized by clonal proliferation of myeloid blasts harboring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anemia, thrombocytopenia, and other nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404391016 | A subtype of acute myeloid leukaemia with recurrent genetic abnormalities, characterised by clonal proliferation of myeloid blasts harbouring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anaemia, thrombocytopenia, and other nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acute myeloid leukaemia with CEBPA somatic mutations | Is a | Acute myeloid leukemia due to recurrent genetic abnormality | false | Inferred relationship | Some | ||
| Acute myeloid leukaemia with CEBPA somatic mutations | Associated morphology | Acute myeloid leukemia with CEBPA mutation (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Acute myeloid leukaemia with CEBPA somatic mutations | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 | |
| Acute myeloid leukaemia with CEBPA somatic mutations | Is a | Acute myeloid leukemia, disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR