Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1198718017 | Upshaw-Schulman syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
1211899017 | Upshaw-Schulman syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
1216561016 | Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
1218052015 | Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
1229241011 | Familial TTP/HUS | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
5150505018 | Congenital ADAMTS-13 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets