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 |
| 351283011 | Fibrinogen abnormality | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 622777017 | Fibrinogen abnormality (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6667661000146118 | afwijking van fibrinogeen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6667671000146112 | afwijking van fibrinogeen (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6667701000146111 | afwijking van stollingsfactor I | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Fibrinogen abnormality | Is a | Blood coagulation disorder | true | Inferred relationship | Some | ||
| Fibrinogen abnormality | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Fibrinogen abnormality | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Fibrinogen abnormality | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Fibrinogen abnormality | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Fibrinogen abnormality | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cryofibrinogenemia | Is a | True | Fibrinogen abnormality | Inferred relationship | Some | |
| Congenital fibrinogen abnormality | Is a | True | Fibrinogen abnormality | Inferred relationship | Some | |
| Acquired fibrinogen abnormality | Is a | True | Fibrinogen abnormality | Inferred relationship | Some | |
| Acquired hypofibrinogenemia | Is a | False | Fibrinogen abnormality | Inferred relationship | Some | |
| Fibrinogen deficiency | Is a | True | Fibrinogen abnormality | Inferred relationship | Some | |
| Acquired afibrinogenemia | Is a | False | Fibrinogen abnormality | Inferred relationship | Some | |
| Factor XIII deficiency disease | Is a | False | Fibrinogen abnormality | Inferred relationship | Some | |
| Afibrinogenemia | Is a | True | Fibrinogen abnormality | Inferred relationship | Some | |
| Hypofibrinogenaemia | Is a | True | Fibrinogen abnormality | Inferred relationship | Some | |
| Hyperfibrinogenemia (disorder) | Is a | True | Fibrinogen abnormality | Inferred relationship | Some |
This concept is not in any reference sets
FHIR