Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347703014 | Autosomal dominant retinitis pigmentosa | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
620067015 | Autosomal dominant retinitis pigmentosa (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant retinitis pigmentosa | Is a | Retinitis pigmentosa | true | Inferred relationship | Existential restriction modifier | ||
Autosomal dominant retinitis pigmentosa | Finding site | Retinal structure | false | Inferred relationship | Existential restriction modifier | ||
Autosomal dominant retinitis pigmentosa | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Autosomal dominant retinitis pigmentosa | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
Autosomal dominant retinitis pigmentosa | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | Is a | True | Autosomal dominant retinitis pigmentosa | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets