Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1767809013 | Hereditary lymphedema type I (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
1773470018 | Hereditary lymphoedema type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1774756010 | Hereditary lymphedema type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1783719015 | Nonne-Milroy lymphoedema | en | Synonym | Active | Case sensitive | SNOMED CT core |
1783720014 | Primary congenital lymphoedema | en | Synonym | Active | Case insensitive | SNOMED CT core |
1783721013 | Milroy lymphoedema | en | Synonym | Active | Case sensitive | SNOMED CT core |
1784105016 | Nonne-Milroy lymphedema | en | Synonym | Active | Case sensitive | SNOMED CT core |
1784106015 | Milroy lymphedema | en | Synonym | Active | Case sensitive | SNOMED CT core |
1784107012 | Primary congenital lymphedema | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set