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 |
| 1230410010 | Factor XII deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1230411014 | Hageman factor deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 78295019 | Factor XII deficiency disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 784389014 | Factor XII deficiency disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor XII deficiency disease | interprète (attribut) | Hemostatic function (observable entity) | true | Inferred relationship | Some | 1 | |
| Factor XII deficiency disease | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 1 | |
| Factor XII deficiency disease | est un(e) (attribut) | Contact factor deficiency | true | Inferred relationship | Some | ||
| Factor XII deficiency disease | est un(e) (attribut) | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| Factor XII deficiency disease | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Factor XII deficiency disease | est défini par la manifestation de (attribut) | constatation sur le système hémostatique | false | Inferred relationship | Some | ||
| Factor XII deficiency disease | localisation d'une constatation (attribut) | Entire hematological system (body structure) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acquired factor XII deficiency disease | est un(e) (attribut) | True | Factor XII deficiency disease | Inferred relationship | Some | |
| Hereditary factor XII deficiency disease | est un(e) (attribut) | True | Factor XII deficiency disease | Inferred relationship | Some |
Reference Sets
FHIR