Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2005. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 2546843015 | Congenital hereditary endothelial dystrophy,CHED 1 (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 2549153018 | Congenital hereditary endothelial dystrophy,CHED 1 | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 2553886018 | congenital hereditary endothelial dystrophy, autosomal dominant form | en | Synonym | Inactive | Entire term case insensitive | SNOMED CT core module | 
| 3644846012 | Congenital hereditary endothelial dystrophy type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 3644847015 | Congenital hereditary endothelial dystrophy autosomal dominant form | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 3644848013 | Congenital hereditary endothelial dystrophy type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 3644852013 | CHED1 - congenital hereditary endothelial dystrophy type 1 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets