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 |
2547521014 | Congenital hereditary endothelial dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
2549868019 | Congenital hereditary endothelial dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2554123017 | CHED-congenital hereditary endothelial dystrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital hereditary endothelial dystrophy type 1 | Is a | True | Congenital hereditary endothelial dystrophy | Inferred relationship | Existential restriction modifier | |
Congenital hereditary endothelial dystrophy type 2 | Is a | True | Congenital hereditary endothelial dystrophy | Inferred relationship | Existential restriction modifier | |
Congenital hereditary endothelial dystrophy and perceptive deafness syndrome | Is a | True | Congenital hereditary endothelial dystrophy | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets