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 |
| 345081017 | Silver disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 618047012 | Silver disease (disorder) | en | Fully specified name | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3701800010 | Autosomal dominant spastic paraplegia type 17 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3701801014 | Autosomal dominant spastic paraplegia type 17 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4674028016 | A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5448822018 | A complex hereditary spastic paraplegia characterised by progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. Association with hand muscles amyotrophy is typical. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5448823011 | A complex hereditary spastic paraplegia characterized by progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. Association with hand muscles amyotrophy is typical. | 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 17 (disorder) | Is a | Disorder primarily affecting the motor pathways | false | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Lower limb structure | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Autosomal dominant hereditary spastic paraplegia | false | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 3 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Autosomal dominant distal hereditary motor neuropathy (disorder) | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Nerve structure | true | Inferred relationship | Some | 4 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 5 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Complicated hereditary spastic paraplegia | false | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Interprets | Movement | false | Inferred relationship | Some | 8 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Structure of right lower limb (body structure) | true | Inferred relationship | Some | 6 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Structure of left lower limb (body structure) | true | Inferred relationship | Some | 7 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Interprets | Movement observable | true | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Has interpretation | Absent | true | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Autosomal dominant complex hereditary spastic paraplegia (disorder) | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Nerve palsy | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Structure of motor nervous system (body structure) | true | Inferred relationship | Some | 8 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)