Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2005. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3644846012 | Congenital hereditary endothelial dystrophy type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644847015 | Congenital hereditary endothelial dystrophy autosomal dominant form | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644848013 | Congenital hereditary endothelial dystrophy type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644852013 | CHED1 - congenital hereditary endothelial dystrophy type 1 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
258931000052111 | medfödd ärftlig endoteldystrofi, dominant form | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Is a | Congenital hereditary endothelial dystrophy (disorder) | true | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy type 1 (disorder) | Associated morphology | kongenital anomali | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Finding site | Corneal structure | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Finding site | Chromosome pair 20 | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy type 1 (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Finding site | Structure of corneal endothelium | false | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Associated morphology | kongenital anomali | false | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy type 1 (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Finding site | Structure of corneal endothelium | true | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Finding site | Chromosome pair 20 | true | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Associated morphology | Cellular AND/OR subcellular abnormality | true | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy type 1 (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy type 1 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets