Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
62890013 | Hereditary acrodermatitis enteropathica | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
62891012 | Primary zinc malabsorption syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
62892017 | Brandt syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
62893010 | Danbolt-Closs syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
62894016 | Hereditary acrodermatitis enterohepatica | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
486788010 | AE - Acrodermatitis enteropathica | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
486789019 | Primary zinc malabsorption | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
486790011 | Danbolt-Close syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
486791010 | Acrodermatitis enteropathica | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
769600013 | Hereditary acrodermatitis enteropathica (disorder) | en | Fully specified name | 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