Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1226074019 | RP - Retinitis pigmentosa | en | Synonym | Active | Case sensitive | SNOMED CT core |
48282015 | Retinitis pigmentosa | en | Synonym | Active | Case insensitive | SNOMED CT core |
759560017 | Retinitis pigmentosa (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Retinitis pigmentosa | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
Retinitis pigmentosa | Is a | Autosomal hereditary disorder | false | Inferred relationship | Some | ||
Retinitis pigmentosa | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa | Finding site | Retinal structure | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa | 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