Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1216410012 | Hereditary haemorrhagic thrombasthenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
1217904013 | Hereditary hemorrhagic thrombasthenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
1228017010 | Glanzmann's syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
196971014 | Glanzmann's thrombasthenia | en | Synonym | Active | Case sensitive | SNOMED CT core |
2646881012 | Glanzmann's disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
54984011 | Hereditary thromboasthenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
54986013 | Glanzmann thromboasthenia | en | Synonym | Active | Case sensitive | SNOMED CT core |
54987016 | Glanzmann-Naegeli disorder | en | Synonym | Active | Case sensitive | SNOMED CT core |
54989018 | Thrombasthenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
764285014 | Glanzmann's thrombasthenia (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set