Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Dysfibrinogenemia | Is a | Congenital fibrinogen abnormality | true | Inferred relationship | Some | ||
Dysfibrinogenemia | Is a | Coagulation factor deficiency syndrome | false | Inferred relationship | Some | ||
Dysfibrinogenemia | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
Dysfibrinogenemia | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Dysfibrinogenemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
Dysfibrinogenemia | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
Dysfibrinogenemia | Is a | Factor I deficiency disease (disorder) | true | Inferred relationship | Some | ||
Dysfibrinogenemia | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
Dysfibrinogenemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Alpha chain defect dysfibrinogenemia | Is a | True | Dysfibrinogenemia | Inferred relationship | Some | |
Beta chain defect dysfibrinogenaemia | Is a | True | Dysfibrinogenemia | Inferred relationship | Some | |
Gamma chain defect dysfibrinogenaemia | Is a | True | Dysfibrinogenemia | Inferred relationship | Some | |
Hereditary dysfibrinogenemia (disorder) | Is a | True | Dysfibrinogenemia | Inferred relationship | Some |
Reference Sets
Belgian subset for medical problems in patient health records