Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347713018 | Hereditary vitreoretinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
620078011 | Hereditary vitreoretinopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6252041000241119 | vitréorétinopathie héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6252051000241116 | VRH - vitréorétinopathie héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
543971000274114 | Hereditäre Vitreoretinopathie | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary vitreoretinopathy | Is a | Disorder of vitreous body | true | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Finding site | Composite structure of hyaluronic acid gel within a stromal network of collagen fibrils | true | Inferred relationship | Some | 1 | |
Hereditary vitreoretinopathy | Is a | Retinopathy | false | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Finding site | Retinal structure | true | Inferred relationship | Some | 2 | |
Hereditary vitreoretinopathy | Is a | Retinal disorder | true | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
Hereditary vitreoretinopathy | Is a | Connective tissue hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial exudative vitreoretinopathy | Is a | True | Hereditary vitreoretinopathy | Inferred relationship | Some | |
Wagner syndrome | Is a | True | Hereditary vitreoretinopathy | Inferred relationship | Some | |
Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis). | Is a | False | Hereditary vitreoretinopathy | Inferred relationship | Some | |
Stickler syndrome | Is a | True | Hereditary vitreoretinopathy | Inferred relationship | Some |
This concept is not in any reference sets