Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
456725016 | Cone dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
709642015 | Cone dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cone dystrophy | Finding site | Cone of retina | true | Inferred relationship | Some | 1 | |
Cone dystrophy | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
Cone dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Cone dystrophy | Finding site | Retinal structure | false | Inferred relationship | Some | 1 | |
Cone dystrophy | Finding site | Retinal structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Achromatopsia | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Blue cone monochromatism | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Progressive cone dystrophy (without rod involvement) | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Cone dystrophy with supernormal rod response | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Retinohepatoendocrinologic syndrome | Is a | True | Cone dystrophy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set