Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3656355013 | Autosomal recessive spastic paraplegia type 62 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3656356014 | Autosomal recessive spastic paraplegia type 62 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3656174014 | A pure or complex form of hereditary spastic paraplegia with characteristics of onset in the first decade of life of spastic paraparesis (more prominent in lower than upper extremities) and unsteady gait, as well as increased deep tendon reflexes, amyotrophy, cerebellar ataxia and flexion contractures of the knees in some. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 62 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 62 | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 62 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 62 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 62 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 62 | Has interpretation | Absent | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 62 | Is a | Hereditary spastic paraplegia | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 62 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 62 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Structure of lower limb | false | 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