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 |
| 1228016018 | Glanzsmann's disease | en | Synonym | Inactive | Initial character 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 |
| 54985012 | Hereditary thromboasthenia, NOS | en | Synonym | Inactive | Initial character 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 |
| 54988014 | Thrombasthenia, NOS | en | Synonym | Inactive | Initial character case insensitive | 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