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 |
7537581000146111 | Grayson-Wilbrandt-corneadystrofie | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
7542531000146114 | corneadystrofie van Grayson-Wilbrandt (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
7542541000146118 | corneadystrofie van Grayson-Wilbrandt | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3312833018 | An extremely rare form of corneal dystrophy with manifestation of variable patterns of opacification in the Bowman layer of the cornea that extend anteriorly into the epithelium with decreased to normal visual acuity. Onset is in the first to second decade of life. Patients develop painful erosions that are less severe than those in Reis-Bucklers corneal dystrophy and Thiel-Behnke corneal dystrophy. Visual acuity is normal or sometimes slightly decreased. The condition has a progressive course. An autosomal dominant pattern of inheritance has been reported. | 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 |
This concept is not in any reference sets