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 |
| 351287012 | Hypodysfibrinogenaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 351288019 | Hypodysfibrinogenemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 622781017 | Hypodysfibrinogenemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypodysfibrinogenaemia | Is a | Congenital fibrinogen abnormality | true | Inferred relationship | Some | ||
| Hypodysfibrinogenaemia | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Hypodysfibrinogenaemia | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Hypodysfibrinogenaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hypodysfibrinogenaemia | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Hypodysfibrinogenaemia | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Hypodysfibrinogenaemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hypodysfibrinogenaemia | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Hypodysfibrinogenaemia | Is a | Fibrinogen deficiency | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR