Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
147324016 | Chronic constitutional pure red cell aplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
147326019 | Chronic constitutional pure red cell anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
147327011 | Congenital erythroid hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
147328018 | Congenital hypoplastic anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
147329014 | Familial hypoplastic anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
2820761015 | Congenital hypoplastic anemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3664230017 | Congenital pure red cell anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3664231018 | Erythrogenesis imperfecta | en | Synonym | Active | Case insensitive | SNOMED CT core |
3664232013 | Congenital pure red cell anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
508242017 | Congenital red cell aplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
508244016 | Congenital hypoplastic anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
508246019 | Chronic constitutional pure red cell anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
508247011 | Familial hypoplastic anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Aase syndrome | Is a | True | Congenital hypoplastic anaemia | Inferred relationship | Some | |
H/O: Diamond-Blackfan anaemia | Associated finding | False | Congenital hypoplastic anaemia | Inferred relationship | Some | 1 |
H/O: Diamond-Blackfan anaemia | Associated finding | True | Congenital hypoplastic anaemia | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set