Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2530854017 | Hereditary disorder of cellular element of blood (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2534319013 | Hereditary disorder of cellular element of blood | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2596661000052110 | ärftlig sjukdom hos cellulärt element i blodet | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary disorder of cellular element of blood (disorder) | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Hereditary disorder of cellular element of blood (disorder) | Is a | Disorder of cellular component of blood (disorder) | true | Inferred relationship | Some | ||
| Hereditary disorder of cellular element of blood (disorder) | Has definitional manifestation | Finding of cellular component of blood (finding) | false | Inferred relationship | Some | ||
| Hereditary disorder of cellular element of blood (disorder) | Finding site | Body system structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary red blood cell disorder (disorder) | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Hereditary white blood cell disorder (disorder) | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Inherited platelet disorder | Is a | False | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Hermansky-Pudlak syndrome | Is a | False | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Radial aplasia-thrombocytopenia syndrome | Is a | False | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Epstein syndrome | Is a | False | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Wiskott-Aldrich syndrome | Is a | False | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Inherited platelet disorder | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| WT limb blood syndrome (disorder) | Is a | False | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Revesz syndrome (disorder) | Is a | False | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Mitochondrial myopathy with sideroblastic anemia syndrome (disorder) | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Aase syndrome | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some | |
| Ghosal hematodiaphyseal dysplasia | Is a | True | Hereditary disorder of cellular element of blood (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR