Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2789363016 | Congenital hypofibrinogenemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2794588013 | Congenital hypofibrinogenemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2794589017 | Congenital hypofibrinogenaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hypofibrinogenemia (disorder) | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 2 | |
| Congenital hypofibrinogenemia (disorder) | interprète (attribut) | Hemostatic function (observable entity) | true | Inferred relationship | Some | 2 | |
| Congenital hypofibrinogenemia (disorder) | est un(e) (attribut) | Hereditary factor I deficiency disease | true | Inferred relationship | Some | ||
| Congenital hypofibrinogenemia (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR