Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3726004011 | Autosomal dominant rhegmatogenous retinal detachment (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3726005012 | Autosomal dominant rhegmatogenous retinal detachment | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant rhegmatogenous retinal detachment | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
Autosomal dominant rhegmatogenous retinal detachment | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Autosomal dominant rhegmatogenous retinal detachment | Is a | Rhegmatogenous retinal detachment | true | Inferred relationship | Existential restriction modifier | ||
Autosomal dominant rhegmatogenous retinal detachment | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Autosomal dominant rhegmatogenous retinal detachment | Associated morphology | Separation | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets