Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3425174013 | Subepithelial mucinous corneal dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3425175014 | Subepithelial mucinous corneal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3425176010 | A very rare form of superficial corneal dystrophy with characteristics of frequent recurrent corneal erosions in the first decade of life and progressive loss of vision. The condition has only been reported in one single family. Painful episodes of recurrent corneal erosions occur in the first decade of life but decrease during adolescence. Later in life, patients are reported to develop subepithelial opacities and a corneal haze. The disease eventually progresses over time leading to corneal opacities and loss of vision. The gene related to this disease has not been mapped to a particular chromosomal locus. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Subepithelial mucinous corneal dystrophy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Subepithelial mucinous corneal dystrophy | Is a | Hereditary corneal dystrophy | true | Inferred relationship | Some | ||
Subepithelial mucinous corneal dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Subepithelial mucinous corneal dystrophy | Finding site | Corneal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set