Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3737335011 | Autosomal recessive spastic paraplegia type 27 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3737336012 | Autosomal recessive spastic paraplegia type 27 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3737340015 | A rare pure or complex hereditary spastic paraplegia with characteristics of variable onset of slowly progressive lower limb spasticity, hyperreflexia and extensor plantar responses, that may be associated with sensorimotor polyneuropathy, decreased vibration sense, lower limb distal muscle wasting, dysarthria and mild to moderate intellectual disability. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 27 | Is a | Hereditary spastic paraplegia | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 27 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 27 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 27 | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 27 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 27 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 27 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 27 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 27 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 27 | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 27 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 27 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 27 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 27 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 27 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 27 | Has interpretation | Absent | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set