Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3637767012 | Autosomal dominant spastic paraplegia type 41 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3637768019 | Autosomal dominant spastic paraplegia type 41 | en | Synonym | Active | Case insensitive | SNOMED CT core |
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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant spastic paraplegia type 41 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 41 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
Autosomal dominant spastic paraplegia type 41 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal dominant spastic paraplegia type 41 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 4 | |
Autosomal dominant spastic paraplegia type 41 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal dominant spastic paraplegia type 41 | Interprets | Movement observable | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 41 | Has interpretation | Absent | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 41 | Is a | Pure hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 41 | Is a | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 41 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 41 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 41 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 41 | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 41 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set