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 |
| 767321000241114 | fundus albipunctatus (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 979841000172111 | fundus albipunctatus | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3655683012 | A rare genetic retinal dystrophy with characteristics of 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 | est un(e) (attribut) | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Fundus albipunctatus | est un(e) (attribut) | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
| Fundus albipunctatus | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
| Fundus albipunctatus | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Fundus albipunctatus | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Fundus albipunctatus | localisation d'une constatation (attribut) | structure de la rétine | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR