Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308959015 | Grayson Wilbrandt dystrophy of cornea (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308960013 | Grayson Wilbrandt corneal dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3312832011 | Grayson Wilbrandt dystrophy of cornea | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401553019 | Grayson-Wilbrandt corneal dystrophy (GWCD) is an extremely rare form of corneal dystrophy characterized by variable patterns of opacification in the Bowman layer of the cornea which extend anteriorly into the epithelium with decreased to normal visual acuity. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401554013 | Grayson-Wilbrandt corneal dystrophy (GWCD) is an extremely rare form of corneal dystrophy characterised by variable patterns of opacification in the Bowman layer of the cornea which extend anteriorly into the epithelium with decreased to normal visual acuity. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Grayson Wilbrandt dystrophy of cornea (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Grayson Wilbrandt dystrophy of cornea (disorder) | Is a | Corneal opacity | true | Inferred relationship | Some | ||
Grayson Wilbrandt dystrophy of cornea (disorder) | Is a | Hereditary corneal dystrophy | true | Inferred relationship | Some | ||
Grayson Wilbrandt dystrophy of cornea (disorder) | Is a | Bowman's membrane finding | true | Inferred relationship | Some | ||
Grayson Wilbrandt dystrophy of cornea (disorder) | Finding site | Anterior limiting lamina of cornea | true | Inferred relationship | Some | 2 | |
Grayson Wilbrandt dystrophy of cornea (disorder) | Finding site | Anterior limiting lamina of cornea | true | Inferred relationship | Some | 3 | |
Grayson Wilbrandt dystrophy of cornea (disorder) | Associated morphology | Opacity | true | Inferred relationship | Some | 2 | |
Grayson Wilbrandt dystrophy of cornea (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)