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 |
| 3638491016 | Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638492011 | Acute myeloid leukaemia with NPM1 somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3638493018 | Acute myeloid leukemia with NPM1 somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3638494012 | Acute myeloid leukemia with nucleophosmin 1 somatic mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638495013 | Acute myeloid leukaemia with nucleophosmin 1 somatic mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638496014 | A subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by clonal proliferation of myeloid blasts harboring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. Patients usually present with leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3638497017 | A subtype of acute myeloid leukaemia with recurrent genetic abnormalities characterised by clonal proliferation of myeloid blasts harbouring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. Patients usually present with leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. | 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 nucleophosmin 1 somatic mutation (disorder) | Is a | Acute myeloid leukemia due to recurrent genetic abnormality | false | Inferred relationship | Some | ||
| Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | Associated morphology | Acute myeloid leukemia with mutated NPM1 (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 | |
| Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | Is a | Acute myeloid leukemia, disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR