Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3637770011 | Autosomal dominant spastic paraplegia type 42 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3637771010 | Autosomal dominant spastic paraplegia type 42 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3637772015 | A pure form of hereditary spastic paraplegia with characteristics of slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood and patients presenting with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and, in rare cases, pes cavus. No abnormalities are noted on magnetic resonance imaging. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant spastic paraplegia type 42 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 42 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
| Autosomal dominant spastic paraplegia type 42 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 42 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 42 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 42 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
| Autosomal dominant spastic paraplegia type 42 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 4 | |
| Autosomal dominant spastic paraplegia type 42 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
| Autosomal dominant spastic paraplegia type 42 | Interprets | Movement observable | true | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 42 | Has interpretation | Absent | true | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 42 | Is a | Pure hereditary spastic paraplegia | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 42 | Is a | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 42 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 42 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 42 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 42 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 42 | Associated morphology | Degeneration | 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
FHIR