Status: current, Primitive. Date: 31-Jan 2015. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3030814014 | Jalili syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3030832014 | Amelogenesis imperfecta co-occurrent with cone rod dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3030889013 | Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Finding site | Structure of hard tissue of tooth | false | Inferred relationship | Some | 1 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Finding site | Enamel structure | true | Inferred relationship | Some | 1 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Is a | Amelogenesis imperfecta | true | Inferred relationship | Some | ||
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 2 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Finding site | Retinal structure | true | Inferred relationship | Some | 2 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 3 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Amelogenesis imperfecta co-occurrent with cone rod dystrophy | Finding site | Structure of hard tissue of tooth | false | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set