Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3424464010 | Multifocal pattern dystrophy simulating Stargardt disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3424466012 | Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3424467015 | Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3424468013 | Multifocal pattern dystrophy simulating fundus flavimaculatus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6967461000146115 | multifocale patroondystrofie van retinaal pigmentepitheel lijkend op fundus flavimaculatus (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6967471000146114 | ziekte van Stargardt simulerende multifocale patroondystrofie van retinaal pigmentepitheel | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6967481000146111 | multifocale patroondystrofie van retinaal pigmentepitheel lijkend op fundus flavimaculatus | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3424465011 | A patterned dystrophy of the retinal pigment epithelium with characteristics of multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease. Usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
| Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) | Is a | Retinal pigment epithelial dystrophy | true | Inferred relationship | Some | ||
| Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
| Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) | Finding site | Structure of retinal pigment epithelium | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR