Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3640263013 | Autosomal dominant spastic paraplegia type 19 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3640264019 | Autosomal dominant spastic paraplegia type 19 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3640265018 | A pure form of hereditary spastic paraplegia with characteristics of a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant spastic paraplegia type 19 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 19 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
Autosomal dominant spastic paraplegia type 19 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 19 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 19 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 19 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal dominant spastic paraplegia type 19 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 4 | |
Autosomal dominant spastic paraplegia type 19 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal dominant spastic paraplegia type 19 | Interprets | Movement observable | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 19 | Has interpretation | Absent | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 19 | Is a | Pure hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 19 | Is a | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 19 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 19 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 19 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 19 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 19 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set