Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 178837018 | Reticular dysgenesis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 363882019 | De Vaal disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 363883012 | Immunoerythromyeloid hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 363884018 | Severe combined immunodeficiency, neutropaenia and thrombocytopaenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 363885017 | SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 363886016 | Congenital aleukia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 363887013 | Reticular dysgenesia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 363888015 | Generalised haematopoietic hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 363889011 | Generalized hematopoietic hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3786555016 | SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3786556015 | Severe combined immunodeficiency, neutropenia and thrombocytopenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 632826011 | Reticular dysgenesis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Reticular dysgenesis with congenital aleucocytosis | Is a | True | Reticular dysgenesis | Inferred relationship | Some | |
| De Vaal's syndrome | Is a | True | Reticular dysgenesis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set