Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2020. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Associated morphology | histiocytose - categorie (afwijkende morfologie) | false | Inferred relationship | Some | 4 | |
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | false | Inferred relationship | Some | 3 | |
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Is a | secundaire hemofagocytaire lymfohistiocytose (aandoening) | false | Inferred relationship | Some | ||
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Due to | Systemic disease | true | Inferred relationship | Some | 1 | |
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Finding site | Mononuclear phagocyte system structure (body structure) | true | Inferred relationship | Some | 2 | |
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Associated morphology | histiocytose - categorie (afwijkende morfologie) | false | Inferred relationship | Some | 2 | |
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 2 | |
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Is a | Haemophagocytic lymphohistiocytosis | true | Inferred relationship | Some | ||
Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Associated morphology | Histiocytic proliferation (morphologic abnormality) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Macrophage activation syndrome due to juvenile systemic onset arthritis | Is a | True | Hemophagocytic lymphohistiocytosis due to systemic disease (disorder) | Inferred relationship | Some |
This concept is not in any reference sets