Status: current, Primitive. Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1198718017 | Upshaw-Schulman syndrome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
1211899017 | Upshaw-Schulman syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1216561016 | Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
1218052015 | Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
1229241011 | Familial TTP/HUS | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5150505018 | Congenital ADAMTS-13 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set