Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2008. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 2547170017 | Corneal endothelial dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 2549502013 | Corneal endothelial dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 2554004014 | Dystrophy of corneal endothelium | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 2554005010 | Endothelial corneal dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Posterior polymorphous corneal dystrophy | Is a | True | Corneal endothelial dystrophy | Inferred relationship | Existential restriction modifier | |
| Congenital hereditary endothelial dystrophy | Is a | True | Corneal endothelial dystrophy | Inferred relationship | Existential restriction modifier | |
| Cogan-Reese syndrome | Is a | False | Corneal endothelial dystrophy | Inferred relationship | Existential restriction modifier | |
| Chandler syndrome | Is a | True | Corneal endothelial dystrophy | Inferred relationship | Existential restriction modifier | |
| X-linked endothelial dystrophy of cornea | Is a | True | Corneal endothelial dystrophy | Inferred relationship | Existential restriction modifier | |
| Congenital hereditary endothelial dystrophy and perceptive deafness syndrome | Is a | False | Corneal endothelial dystrophy | Inferred relationship | Existential restriction modifier | 
This concept is not in any reference sets