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 |
121372015 | Hereditary elliptocytosis due to beta spectrin defect in self-association | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
813421012 | Hereditary elliptocytosis due to beta spectrin defect in self-association (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 |
Hereditary elliptocytosis due to beta spectrin defect in self-association | a pour interprétation (attribut) | présent (valeur de l'attribut) | true | Inferred relationship | Some | 3 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | interprète (attribut) | Hemolysis (observable entity) | true | Inferred relationship | Some | 3 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | localisation d'une constatation (attribut) | Erythrocyte | true | Inferred relationship | Some | 4 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | morphologie associée (attribut) | Elliptocyte (cell) | true | Inferred relationship | Some | 4 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | survenue (attribut) | congénital | true | Inferred relationship | Some | 4 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | est défini par la manifestation de (attribut) | Erythropenia | false | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | est un(e) (attribut) | Hereditary disorder of hematologic system | false | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | est un(e) (attribut) | Hereditary elliptocytosis | true | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | est un(e) (attribut) | anémie causée par une anomalie constitutionnelle des érythrocytes | true | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 1 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | interprète (attribut) | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 1 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 2 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | interprète (attribut) | Red blood cell count | true | Inferred relationship | Some | 2 | |
Hereditary elliptocytosis due to beta spectrin defect in self-association | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | interprète (attribut) | spectrine | false | Inferred relationship | Some | ||
Hereditary elliptocytosis due to beta spectrin defect in self-association | localisation d'une constatation (attribut) | Erythrocyte | false | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets