Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
69728015 | Hereditary retinal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
778627018 | Hereditary retinal dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary retinal dystrophy | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
Hereditary retinal dystrophy | Is a | Hereditary disease | false | Inferred relationship | Some | ||
Hereditary retinal dystrophy | Is a | Retinal dystrophy | true | Inferred relationship | Some | ||
Hereditary retinal dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Hereditary retinal dystrophy | Finding site | Retinal structure | true | Inferred relationship | Some | 1 | |
Hereditary retinal dystrophy | Finding site | Retinal structure | false | Inferred relationship | Some |
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