Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3655681014 | Fundus albipunctatus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3655682019 | Fundus albipunctatus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5404404017 | Fundus albipunctatus is a rare, genetic retinal dystrophy disorder characterized by the presence of numerous small, round, yellowish-white retinal lesions that are distributed throughout the retina but spare the fovea. Patients present in childhood with non-progressive night blindness with prolonged cone and rod adaptation times. The macula may or may not be involved, which may result in a decrease of central visual acuity with age. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404405016 | Fundus albipunctatus is a rare, genetic retinal dystrophy disorder characterised by the presence of numerous small, round, yellowish-white retinal lesions that are distributed throughout the retina but spare the fovea. Patients present in childhood with non-progressive night blindness with prolonged cone and rod adaptation times. The macula may or may not be involved, which may result in a decrease of central visual acuity with age. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Fundus albipunctatus | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
Fundus albipunctatus | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
Fundus albipunctatus | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
Fundus albipunctatus | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Fundus albipunctatus | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Fundus albipunctatus | Finding site | Retinal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)