Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2620827010 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to triosephosphate isomerase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2620828017 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2914313017 | Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2914791016 | Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3780589014 | Hereditary nonspherocytic haemolytic anaemia due to triosephosphate isomerase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 493971019 | Triosephosphate deficiency anaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 74466015 | HNSHA due to triosephosphate isomerase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 74467012 | Triosephosphate deficiency anemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | a pour interprétation (attribut) | présent (valeur de l'attribut) | true | Inferred relationship | Some | 3 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | interprète (attribut) | Hemolysis (observable entity) | true | Inferred relationship | Some | 3 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est un(e) (attribut) | Hereditary nonspherocytic haemolytic anaemia | true | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | Associated aetiologic finding | Enzymopathy | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | Associated aetiologic finding | Triose phosphate isomerase deficiency | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est un(e) (attribut) | anomalie congénitale du système hématopoïétique | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est un(e) (attribut) | Anemia due to enzyme deficiency | true | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est un(e) (attribut) | Inborn error of metabolism | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est un(e) (attribut) | Hereditary disorder of hematologic system | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est un(e) (attribut) | Erythrocyte enzyme deficiency | true | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est défini par la manifestation de (attribut) | Erythropenia | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | Due to | Triose phosphate isomerase deficiency | true | Inferred relationship | Some | 5 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | est défini par la manifestation de (attribut) | Hemolysis | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 1 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | interprète (attribut) | Red blood cell count | true | Inferred relationship | Some | 1 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 2 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | interprète (attribut) | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | localisation d'une constatation (attribut) | Erythrocyte | true | Inferred relationship | Some | 4 | |
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) | interprète (attribut) | Erythrocyte destruction, function (observable entity) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR