Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1001251000172113 | SPG41 - spastic paraplegia type 41 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3637767012 | Autosomal dominant spastic paraplegia type 41 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3637768019 | Autosomal dominant spastic paraplegia type 41 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
765511000241116 | paraplégie spastique autosomique dominante type 41 (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
977961000172113 | paraplégie spastique autosomique dominante type 41 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3637769010 | A pure form of hereditary spastic paraplegia with onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant spastic paraplegia type 41 (disorder) | morphologie associée (attribut) | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 41 (disorder) | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 3 | |
Autosomal dominant spastic paraplegia type 41 (disorder) | est un(e) (attribut) | Pure hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 41 (disorder) | est un(e) (attribut) | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 41 (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 41 (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 41 (disorder) | localisation d'une constatation (attribut) | membre inférieur | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 41 (disorder) | morphologie associée (attribut) | dégénérescence | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 41 (disorder) | localisation d'une constatation (attribut) | moelle spinale (structure corporelle) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets