Status: current, Primitive. Date: 31-Jul 2007. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1222141018 | Factor XIII deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
31367019 | Factor XIII deficiency disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
31369016 | Fibrin stabilizing factor deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
478723018 | Fibrin stabilising factor deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
746118017 | Factor XIII deficiency disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary factor I deficiency disease | Is a | False | Factor XIII deficiency disease | Inferred relationship | Some | |
Hereditary factor XIII deficiency disease | Is a | True | Factor XIII deficiency disease | Inferred relationship | Some | |
Acquired factor XIII deficiency disease | Is a | True | Factor XIII deficiency disease | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set