Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3759543016 | Autosomal dominant spastic paraplegia type 38 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3759544010 | Autosomal dominant spastic paraplegia type 38 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3759545011 | A complex hereditary spastic paraplegia with characteristics of mild to severe lower limbs spasticity, hyperreflexia, extensor plantar responses, pes cavus and significant wasting and weakness of the small hand muscles. Impaired vibration sensation, temporal lobe epilepsy and cognitive dysfunction were also reported. | 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 38 (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 38 (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 38 (disorder) | est un(e) (attribut) | Complicated hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 38 (disorder) | est un(e) (attribut) | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 38 (disorder) | localisation d'une constatation (attribut) | moelle spinale (structure corporelle) | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 38 (disorder) | morphologie associée (attribut) | dégénérescence | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 38 (disorder) | localisation d'une constatation (attribut) | membre inférieur | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 38 (disorder) | morphologie associée (attribut) | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 38 (disorder) | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets