Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3654873015 | Autosomal recessive spastic paraplegia type 35 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3654874014 | Autosomal recessive spastic paraplegia type 35 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3654567011 | A rare form of hereditary spastic paraplegia with characteristics of childhood (exceptionally adolescent) onset of a complex phenotype presenting with lower limb (followed by upper limb) spasticity with hyperreflexia and extensor plantar responses, with additional manifestations including progressive dysarthria, dystonia, mild cognitive decline, extrapyramidal features, optic atrophy and seizures. White matter abnormalities and brain iron accumulation have also been observed on brain magnetic resonance imaging. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 35 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 35 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 35 | Is a | Complicated hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 35 | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 35 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 35 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 35 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 35 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 35 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 35 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 35 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 35 | Has interpretation | Absent | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 35 | Is a | Hereditary spastic paraplegia | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 35 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 35 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 35 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 35 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 35 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 35 | 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