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 |
| 1206544013 | Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 482176016 | Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 754820012 | Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | a pour interprétation (attribut) | présent (valeur de l'attribut) | true | Inferred relationship | Some | 4 | |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | interprète (attribut) | Hemolysis (observable entity) | true | Inferred relationship | Some | 4 | |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est un(e) (attribut) | Hereditary nonspherocytic haemolytic anaemia | true | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est un(e) (attribut) | Hereditary disorder of hematologic system | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est un(e) (attribut) | anomalie congénitale du système hématopoïétique | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | localisation d'une constatation (attribut) | Erythrocyte | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est défini par la manifestation de (attribut) | Erythropenia | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est un(e) (attribut) | Congenital anemia | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est défini par la manifestation de (attribut) | Hemolysis | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est un(e) (attribut) | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 1 | |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 2 | |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | interprète (attribut) | Red blood cell count | true | Inferred relationship | Some | 1 | |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | interprète (attribut) | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | interprète (attribut) | Erythrocyte destruction, function (observable entity) | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | est un(e) (attribut) | Congenital haemolytic anaemia | true | Inferred relationship | Some | ||
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | localisation d'une constatation (attribut) | Erythrocyte | true | Inferred relationship | Some | 3 | |
| Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism | survenue (attribut) | congénital | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
FHIR