Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3737478019 | O'Donnell Pappas syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3737479010 | Foveal hypoplasia with presenile cataract syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3737480013 | Foveal hypoplasia with presenile cataract syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
12576261000146115 | syndroom van foveale hypoplasie en preseniel cataract (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
12576271000146114 | syndroom van foveale hypoplasie en preseniel cataract | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3737481012 | A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus and/or optic nerve hypoplasia may also be present. Caused by heterozygous mutation in the PAX6 gene on chromosome 11p13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Foveal hypoplasia with presenile cataract syndrome | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Foveal hypoplasia with presenile cataract syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Foveal hypoplasia with presenile cataract syndrome | Is a | Congenital hypoplasia of fovea centralis (disorder) | true | Inferred relationship | Some | ||
Foveal hypoplasia with presenile cataract syndrome | Associated morphology | cataract | false | Inferred relationship | Some | 2 | |
Foveal hypoplasia with presenile cataract syndrome | Is a | Congenital nystagmus | true | Inferred relationship | Some | ||
Foveal hypoplasia with presenile cataract syndrome | Is a | Presenile cataract | true | Inferred relationship | Some | ||
Foveal hypoplasia with presenile cataract syndrome | Finding site | Structure of fovea centralis | true | Inferred relationship | Some | 1 | |
Foveal hypoplasia with presenile cataract syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Foveal hypoplasia with presenile cataract syndrome | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Foveal hypoplasia with presenile cataract syndrome | Interprets | Ocular motility observable | true | Inferred relationship | Some | 3 | |
Foveal hypoplasia with presenile cataract syndrome | Finding site | Lens clear | true | Inferred relationship | Some | 2 | |
Foveal hypoplasia with presenile cataract syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Foveal hypoplasia with presenile cataract syndrome | Associated morphology | Opacity | true | Inferred relationship | Some | 2 | |
Foveal hypoplasia with presenile cataract syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets