Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 48282015 | Retinitis pigmentosa | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 759560017 | Retinitis pigmentosa (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 1226074019 | RP - Retinitis pigmentosa | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Retinitis pigmentosa | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Existential restriction modifier | ||
| Retinitis pigmentosa | Is a | Autosomal hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Retinitis pigmentosa | Finding site | Retinal structure | false | Inferred relationship | Existential restriction modifier | ||
| Retinitis pigmentosa | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Retinitis pigmentosa | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 1 | 
This concept is not in any reference sets