Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital fibrinogen abnormality | Is a | Fibrinogen abnormality | true | Inferred relationship | Some | ||
Congenital fibrinogen abnormality | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
Congenital fibrinogen abnormality | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
Congenital fibrinogen abnormality | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital fibrinogen abnormality | Finding site | Body system structure | false | Inferred relationship | Some | ||
Congenital fibrinogen abnormality | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
Congenital fibrinogen abnormality | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Congenital fibrinogen abnormality | Interprets | Hemostatic function | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hypofibrinogenaemia | Is a | False | Congenital fibrinogen abnormality | Inferred relationship | Some | |
Hypodysfibrinogenaemia | Is a | True | Congenital fibrinogen abnormality | Inferred relationship | Some | |
Dysfibrinogenemia | Is a | True | Congenital fibrinogen abnormality | Inferred relationship | Some | |
Hereditary factor I deficiency disease | Is a | True | Congenital fibrinogen abnormality | Inferred relationship | Some |
This concept is not in any reference sets