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 |
| 1234012018 | Stuart-Prower factor deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 127274011 | Factor X deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3036019012 | Factor 10 deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 817385017 | Factor X deficiency (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 X deficiency | interprète (attribut) | Hemostatic function (observable entity) | true | Inferred relationship | Some | 1 | |
| Factor X deficiency | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 1 | |
| Factor X deficiency | est un(e) (attribut) | Prothrombin complex deficiency | true | Inferred relationship | Some | ||
| Factor X deficiency | est un(e) (attribut) | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| Factor X deficiency | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Factor X deficiency | est défini par la manifestation de (attribut) | constatation sur le système hémostatique | false | Inferred relationship | Some | ||
| Factor X deficiency | localisation d'une constatation (attribut) | Entire hematological system (body structure) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Factor X deficiency due to systemic amyloidosis | est un(e) (attribut) | True | Factor X deficiency | Inferred relationship | Some | |
| Acquired factor X deficiency disease | est un(e) (attribut) | True | Factor X deficiency | Inferred relationship | Some | |
| Hereditary factor X deficiency disease | est un(e) (attribut) | True | Factor X deficiency | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR