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 |
3759763014 | Autosomal dominant spastic paraplegia type 13 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3759764015 | Autosomal dominant spastic paraplegia type 13 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3759492012 | A rare hereditary spastic paraplegia with characteristics of progressive spastic paraplegia with pyramidal signs in the lower limbs, decreased vibration sense, and increased reflexes in the upper limbs. Caused by heterozygous mutation in the HSPD1 on chromosome 2q33. | 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 13 (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 13 (disorder) | localisation d'une constatation (attribut) | moelle spinale (structure corporelle) | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 13 (disorder) | morphologie associée (attribut) | dégénérescence | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 13 (disorder) | est un(e) (attribut) | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 13 (disorder) | localisation d'une constatation (attribut) | membre inférieur | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 13 (disorder) | morphologie associée (attribut) | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 13 (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