Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3654867016 | Spastic paraplegia, retinal degeneration syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3654869018 | Kjellin syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3654870017 | Autosomal recessive spastic paraplegia type 15 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3654871018 | Hereditary spastic paraparesis type 15 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3654872013 | Autosomal recessive spastic paraplegia type 15 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3654868014 | A complex form of hereditary spastic paraplegia with characteristics of a childhood to adulthood onset of slowly progressive lower limb spasticity (resulting in gait disturbance, extensor plantar responses and decreased vibration sense) associated with mild intellectual disability, mild cerebellar ataxia, peripheral neuropathy (with distal upper limb amyotrophy) and retinal degeneration. Thin corpus callosum is a common imaging finding. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive spastic paraplegia type 15 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Autosomal recessive spastic paraplegia type 15 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
| Autosomal recessive spastic paraplegia type 15 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
| Autosomal recessive spastic paraplegia type 15 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
| Autosomal recessive spastic paraplegia type 15 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 2 | |
| Autosomal recessive spastic paraplegia type 15 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
| Autosomal recessive spastic paraplegia type 15 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
| Autosomal recessive spastic paraplegia type 15 | Has interpretation | Absent | true | Inferred relationship | Some | 4 | |
| Autosomal recessive spastic paraplegia type 15 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
| Autosomal recessive spastic paraplegia type 15 | Is a | Complicated hereditary spastic paraplegia | true | Inferred relationship | Some | ||
| Autosomal recessive spastic paraplegia type 15 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Autosomal recessive spastic paraplegia type 15 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
| Autosomal recessive spastic paraplegia type 15 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Autosomal recessive spastic paraplegia type 15 | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
| Autosomal recessive spastic paraplegia type 15 | 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
FHIR