Status: current, Defined. Date: 31-Jan 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
129114016 | Hereditary corneal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
818666013 | Hereditary corneal dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary corneal dystrophy | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
Hereditary corneal dystrophy | Is a | Corneal dystrophy | true | Inferred relationship | Some | ||
Hereditary corneal dystrophy | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Hereditary corneal dystrophy | Finding site | Corneal structure | false | Inferred relationship | Some | 1 | |
Hereditary corneal dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Hereditary corneal dystrophy | Finding site | Corneal structure | true | Inferred relationship | Some | 1 |
Reference Sets
Emergency department reference set
Australian emergency department reference set
NSW Emergency Department reference set
Clinical finding foundation reference set
Emergency department diagnosis reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
REPLACED BY association reference set