Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3656373011 | Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3656374017 | Spinocerebellar ataxia with axonal neuropathy type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3656375016 | A rare genetic neurological disorder characterised by late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations in upper and lower extremities. Gaze nystagmus, cerebellar dysarthria, peripheral neuropathy, steppage gait and pes cavus develop as disease progresses. Cerebellar atrophy (especially of the vermis) is present in all affected individuals. Additional reported manifestations include seizures, mild brain atrophy, mild hypercholesterolaemia and borderline hypoalbuminaemia. | en | Definition | Active | Case sensitive | SNOMED CT core |
3656376015 | A rare genetic neurological disorder characterized by late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations in upper and lower extremities. Gaze nystagmus, cerebellar dysarthria, peripheral neuropathy, steppage gait and pes cavus develop as disease progresses. Cerebellar atrophy (especially of the vermis) is present in all affected individuals. Additional reported manifestations include seizures, mild brain atrophy, mild hypercholesterolemia and borderline hypoalbuminemia. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Spinocerebellar ataxia with axonal neuropathy type 1 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 | |
Spinocerebellar ataxia with axonal neuropathy type 1 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Spinocerebellar ataxia with axonal neuropathy type 1 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Spinocerebellar ataxia with axonal neuropathy type 1 | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Spinocerebellar ataxia with axonal neuropathy type 1 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Spinocerebellar ataxia with axonal neuropathy type 1 | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Spinocerebellar ataxia with axonal neuropathy type 1 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Spinocerebellar ataxia with axonal neuropathy type 1 | Finding site | Cerebellar structure | false | Inferred relationship | Some | 2 | |
Spinocerebellar ataxia with axonal neuropathy type 1 | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Spinocerebellar ataxia with axonal neuropathy type 1 | Finding site | Spinal cord structure | 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