Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. 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 |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hereditary endothelial dystrophy type 1 | Is a | Congenital hereditary endothelial dystrophy (disorder) | false | Inferred relationship | Some | ||
| Congenital hereditary endothelial dystrophy type 1 | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Congenital hereditary endothelial dystrophy type 1 | Finding site | Corneal structure | false | Inferred relationship | Some | 1 | |
| Congenital hereditary endothelial dystrophy type 1 | Finding site | Chromosome pair 20 | false | Inferred relationship | Some | 1 | |
| Congenital hereditary endothelial dystrophy type 1 | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Congenital hereditary endothelial dystrophy type 1 | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
| Congenital hereditary endothelial dystrophy type 1 | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
| Congenital hereditary endothelial dystrophy type 1 | Finding site | Structure of corneal endothelium | false | Inferred relationship | Some | 2 | |
| Congenital hereditary endothelial dystrophy type 1 | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | ||
| Congenital hereditary endothelial dystrophy type 1 | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
| Congenital hereditary endothelial dystrophy type 1 | Finding site | Structure of corneal endothelium | false | Inferred relationship | Some | 1 | |
| Congenital hereditary endothelial dystrophy type 1 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Congenital hereditary endothelial dystrophy type 1 | Finding site | Chromosome pair 20 | false | Inferred relationship | Some | 2 | |
| Congenital hereditary endothelial dystrophy type 1 | Associated morphology | Cellular AND/OR subcellular abnormality | false | Inferred relationship | Some | 2 | |
| Congenital hereditary endothelial dystrophy type 1 | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
| Congenital hereditary endothelial dystrophy type 1 | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
REPLACED BY association reference set (foundation metadata concept)
FHIR