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 |
2553628017 | Congenital hereditary endothelial dystrophy, autosomal recessive form | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3776017011 | Congenital hereditary endothelial dystrophy type 2 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3776018018 | CHED II - Congenital hereditary endothelial dystrophy II | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3776019014 | Congenital hereditary endothelial dystrophy type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets