Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3640266017 | Autosomal recessive spastic paraplegia type 28 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3640267014 | Autosomal recessive spastic paraplegia type 28 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3640268016 | A pure form of hereditary spastic paraplegia with a childhood or adolescent onset of slowly progressive, pure crural muscle spastic paraparesis which manifests with mild lower limb weakness, gait difficulties, extensor plantar responses, and hyperreflexia of lower extremities. Less common manifestations reported include cerebellar oculomotor disturbance with saccadic eye pursuit, pes cavus and scoliosis. Some patients also present pin and vibration sensory loss in distal legs. The disease is caused by homozygous or compound heterozygous mutation in the DDHD1 gene on chromosome 14q22. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 28 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 28 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 28 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 28 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 28 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 28 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 28 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 28 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 28 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 28 | Interprets | Movement observable | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 28 | Has interpretation | Absent | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 28 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 28 | Is a | Pure hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 28 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 28 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 28 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 28 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 28 | 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
Description inactivation indicator reference set