Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2161483018 | Hereditary angioedema - type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
351542014 | Hereditary angioneurotic edema - type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
351543016 | Hereditary angio-oedema - type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
351544010 | Hereditary angioneurotic oedema - type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
351545011 | C1 esterase inhibitor deficiency - type 2 | en | Synonym | Active | Case sensitive | SNOMED CT core |
351546012 | Hereditary C1 esterase inactivity | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
351547015 | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
622965015 | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder) | en | Fully specified name | 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
Problem/Diagnosis reference set