Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3467558011 | Autosomal recessive spastic paraplegia type 25 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3467559015 | Autosomal recessive spastic paraplegia type 25 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3467560013 | Autosomal recessive spastic paraplegia disc herniation syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3467561012 | A rare complex type of hereditary spastic paraplegia with characteristics of adult-onset spastic paraplegia associated with spinal pain that radiates to the upper or lower limbs and is related to disk herniation (with minor spondylosis), as well as mild sensorimotor neuropathy. The phenotype has been mapped to a locus on chromosome 6q23-q24.1. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 25 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 25 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 25 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 25 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 25 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 25 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 25 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 25 | Has interpretation | Absent | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 25 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 25 | Is a | Complicated hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 25 | Occurrence | Congenital | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 25 | Finding site | Structure of lower limb | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 25 | Associated morphology | Degeneration | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 25 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 25 | Finding site | Cerebellar structure | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 25 | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 25 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 25 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 25 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 25 | Finding site | Structure of lower limb | 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