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 |
3434964012 | Helicoid peripapillary chorioretinal degeneration (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434965013 | Helicoid peripapillary chorioretinal degeneration | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434966014 | Atrophia areata | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434967017 | Sveinsson chorioretinal atrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403323019 | Helicoid peripapillary chorioretinal degeneration is a rare autosomal dominantly inherited chorioretinal degeneration disease, presenting at birth or infancy, characterized by progressive bilateral retinal and choroidal atrophy, appearing as lesions on the optic nerve and peripheral ocular fundus and leading to central vision loss. Congenital anterior polar cataracts are sometimes associated with this disease. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403324013 | Helicoid peripapillary chorioretinal degeneration is a rare autosomal dominantly inherited chorioretinal degeneration disease, presenting at birth or infancy, characterised by progressive bilateral retinal and choroidal atrophy, appearing as lesions on the optic nerve and peripheral ocular fundus and leading to central vision loss. Congenital anterior polar cataracts are sometimes associated with this disease. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Helicoid peripapillary chorioretinal degeneration (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Helicoid peripapillary chorioretinal degeneration (disorder) | Is a | Chorioretinal atrophy | true | Inferred relationship | Some | ||
Helicoid peripapillary chorioretinal degeneration (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Helicoid peripapillary chorioretinal degeneration (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 | |
Helicoid peripapillary chorioretinal degeneration (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 3 | |
Helicoid peripapillary chorioretinal degeneration (disorder) | Finding site | Peripapillary retina | true | Inferred relationship | Some | 2 | |
Helicoid peripapillary chorioretinal degeneration (disorder) | Finding site | Peripapillary choroid | true | Inferred relationship | Some | 3 | |
Helicoid peripapillary chorioretinal degeneration (disorder) | Is a | Peripapillary atrophy (finding) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
Description inactivation indicator reference set