Status: current, Primitive. Date: 31-Jul 2005. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2547521014 | Congenital hereditary endothelial dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2549868019 | Congenital hereditary endothelial dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
2554123017 | CHED-congenital hereditary endothelial dystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Corneal dystrophy and perceptive deafness syndrome | Is a | True | Congenital hereditary endothelial dystrophy | Inferred relationship | Some | |
Congenital hereditary endothelial dystrophy type 1 | Is a | True | Congenital hereditary endothelial dystrophy | Inferred relationship | Some | |
Congenital hereditary endothelial dystrophy type 2 | Is a | True | Congenital hereditary endothelial dystrophy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set