Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3447950017 | Sporadic Blau syndrome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3447951018 | Sporadic Blau syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3447952013 | Early onset sarcoidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3447953015 | A rare systemic inflammatory disease with characteristics of early onset granulomatous arthritis, uveitis and skin rash. There are familial and sporadic forms of the same disease. The disease is due to an inherited or de novo mutation in the NOD2 gene (16q12), responsible for alterations in the innate immune response, inflammation and cell death. | en | Definition | 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
Musculoskeletal finding reference set
Problem/Diagnosis reference set