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