Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 147324016 | Chronic constitutional pure red cell aplasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 147325015 | Diamond-Blackfan anemia | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT core module |
| 147326019 | Chronic constitutional pure red cell anemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 147327011 | Congenital erythroid hypoplasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 147328018 | Congenital hypoplastic anemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 147329014 | Familial hypoplastic anemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 508242017 | Congenital red cell aplasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 508243010 | Diamond-Blackfan syndrome | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT core module |
| 508244016 | Congenital hypoplastic anaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 508245015 | Diamond-Blackfan anaemia | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT core module |
| 508246019 | Chronic constitutional pure red cell anaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 508247011 | Familial hypoplastic anaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 831625013 | Chronic constitutional pure red cell aplasia (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 2820761015 | Congenital hypoplastic anemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3664230017 | Congenital pure red cell anemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3664231018 | Erythrogenesis imperfecta | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3664232013 | Congenital pure red cell anaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 223531000000112 | Blackfan - Diamond syndrome | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT United Kingdom Edition module |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| History of Diamond-Blackfan anemia | Associated finding | False | Congenital hypoplastic anemia | Inferred relationship | Existential restriction modifier | 1 |
| History of Diamond-Blackfan anemia | Associated finding | True | Congenital hypoplastic anemia | Inferred relationship | Existential restriction modifier | 1 |
| Aase syndrome | Is a | True | Congenital hypoplastic anemia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets