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FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR
© HL7.org
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Server Home |
FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR Version n/a
User: [n/a]
Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 442184016 | Normocytic anaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 442185015 | Normocytic anemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 696722016 | Normocytic anemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1852581000195111 | anemia normocitica | it | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 304071000077118 | anémie normocytaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 906771000195116 | Normozytäre Anämie | de | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Normocytic anaemia | Is a | Anemia | true | Inferred relationship | Some | ||
| Normocytic anaemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Normocytic anaemia | Finding site | Erythrocyte (cell) | false | Inferred relationship | Some | ||
| Normocytic anaemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Normocytic anaemia | Has definitional manifestation | érythropénie | false | Inferred relationship | Some | ||
| Normocytic anaemia | Has interpretation | Below reference range | false | Inferred relationship | Some | 1 | |
| Normocytic anaemia | Interprets | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 1 | |
| Normocytic anaemia | Has interpretation | Below reference range | false | Inferred relationship | Some | 2 | |
| Normocytic anaemia | Interprets | Red blood cell count | false | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Normocytic anemia due to aplasia | Is a | True | Normocytic anaemia | Inferred relationship | Some | |
| Normocytic anaemia following acute bleed | Is a | True | Normocytic anaemia | Inferred relationship | Some | |
| Normocytic anemia due to chronic blood loss | Is a | True | Normocytic anaemia | Inferred relationship | Some | |
| A rare congenital disorder of glycosylation caused by mutations in the CAD gene and characterized by epileptic encephalopathy, global developmental delay, normocytic anemia and anisopoikilocytosis. Loss of acquired skills in early childhood is present and natural disease course can be lethal in early childhood. | Is a | True | Normocytic anaemia | Inferred relationship | Some |
This concept is not in any reference sets