Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
456725016 | Cone dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
709642015 | Cone dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5210901000241112 | dystrophie des cônes | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cone dystrophy | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
Cone dystrophy | Finding site | Retinal structure | false | 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 | Cone of retina | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Progressive cone dystrophy (without rod involvement) | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Cone dystrophy with supernormal rod response (disorder) | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Retinohepatoendocrinologic syndrome (disorder) | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Achromatopsia | Is a | True | Cone dystrophy | Inferred relationship | Some | |
Blue cone monochromatism (disorder) | Is a | True | Cone dystrophy | Inferred relationship | Some |
This concept is not in any reference sets