Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3702254017 | Autosomal recessive spastic paraplegia type 70 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3702255016 | Autosomal recessive spastic paraplegia type 70 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3702256015 | A very rare complex subtype of hereditary spastic paraplegia that presents in infancy with delayed motor development (crawling, walking) and has characteristics of lower limb spasticity, increased deep tendon reflexes, extensor plantar responses, impaired vibratory sensation at ankles, amyotrophy and borderline intellectual disability. Additional signs may include gait disturbances, Achilles tendon contractures, and scoliosis and cerebellar abnormalities. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 70 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 70 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 70 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 70 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 70 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 70 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 70 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 70 | Has interpretation | Absent | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 70 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 70 | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 70 | Is a | Complicated hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 70 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 70 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 70 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 70 | Occurrence | Congenital | 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