Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 351285016 | Hypofibrinogenaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 351286015 | Hypofibrinogenemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 622779019 | Hypofibrinogenemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5784781000172113 | hypofibrinogénémie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 8987351000172111 | diminution du taux de fibrinogène plasmatique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4357351000172111 | hypofibrinogenemie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypofibrinogenaemia | Is a | Congenital fibrinogen abnormality | false | Inferred relationship | Some | ||
| Hypofibrinogenaemia | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Hypofibrinogenaemia | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Hypofibrinogenaemia | Is a | Fibrinogen abnormality | true | Inferred relationship | Some | ||
| Hypofibrinogenaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hypofibrinogenaemia | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Hypofibrinogenaemia | Is a | Factor I deficiency disease (disorder) | true | Inferred relationship | Some | ||
| Hypofibrinogenaemia | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Hypofibrinogenaemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acquired hypofibrinogenemia | Is a | True | Hypofibrinogenaemia | Inferred relationship | Some | |
| Parturient hemorrhage associated with hypofibrinogenemia | Associated with | False | Hypofibrinogenaemia | Inferred relationship | Some | 2 |
| Antepartum hemorrhage with hypofibrinogenemia | Associated with | False | Hypofibrinogenaemia | Inferred relationship | Some | 1 |
| Antepartum hemorrhage with hypofibrinogenemia | Is a | True | Hypofibrinogenaemia | Inferred relationship | Some | |
| Parturient hemorrhage associated with hypofibrinogenemia | Is a | True | Hypofibrinogenaemia | Inferred relationship | Some |
Reference Sets
Belgian subset for medical problems in patient health records
FHIR