Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3316670010 | Benign concentric annular macular dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3316671014 | Benign concentric annular macular dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
4361404018 | A progressive autosomal dominant macular dystrophy with characteristics of parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Benign concentric annular macular dystrophy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Benign concentric annular macular dystrophy | Is a | Hereditary macular dystrophy | true | Inferred relationship | Some | ||
Benign concentric annular macular dystrophy | Finding site | Macula lutea structure | false | Inferred relationship | Some | ||
Benign concentric annular macular dystrophy | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
Benign concentric annular macular dystrophy | Finding site | Retinal structure | false | Inferred relationship | Some | 2 | |
Benign concentric annular macular dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Benign concentric annular macular dystrophy | Finding site | Macula lutea structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set