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 |
| 1000841000172118 | dystrophie réticulée de l'épithélium pigmentaire rétinien | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3424856011 | Reticular dystrophy of retinal pigment epithelium (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3424857019 | Reticular dystrophy of retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 759671000241118 | dystrophie réticulée de l'épithélium pigmentaire rétinien (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3424858012 | A patterned dystrophy of the retinal pigment epithelium with a progressive course. The disease is characterized by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. Sometimes associated with scleral staphyloma, choroidal neovascularization, convergent strabismus, spherophakia with myopia and luxated lenses and partial atrophy of the iris. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3424859016 | A patterned dystrophy of the retinal pigment epithelium with a progressive course. The disease is characterised by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. Sometimes associated with scleral staphyloma, choroidal neovascularisation, convergent strabismus, spherophakia with myopia and luxated lenses and partial atrophy of the iris. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| dystrophie réticulée de l'épithélium pigmentaire rétinien | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| dystrophie réticulée de l'épithélium pigmentaire rétinien | est un(e) (attribut) | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
| dystrophie réticulée de l'épithélium pigmentaire rétinien | est un(e) (attribut) | Retinal pigment epithelial dystrophy (disorder) | true | Inferred relationship | Some | ||
| dystrophie réticulée de l'épithélium pigmentaire rétinien | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| dystrophie réticulée de l'épithélium pigmentaire rétinien | localisation d'une constatation (attribut) | 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