Status: current, Primitive. Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4964981014 | Spinocerebellar ataxia type 42 | en | Synonym | Active | Case insensitive | SNOMED CT core |
4964982019 | Spinocerebellar ataxia type 42 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4964983012 | A rare autosomal dominant cerebellar ataxia with characteristics of pure and slowly progressive cerebellar signs combining gait instability, dysarthria, nystagmus, saccadic eye movements and diplopia. Less frequent clinical signs and symptoms include spasticity, hyperreflexia, decreased distal vibration sense, urinary urgency or incontinence and postural tremor. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Spinocerebellar ataxia type 42 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Spinocerebellar ataxia type 42 | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Spinocerebellar ataxia type 42 | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Spinocerebellar ataxia type 42 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
Spinocerebellar ataxia type 42 | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Spinocerebellar ataxia type 42 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Spinocerebellar ataxia type 42 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Spinocerebellar ataxia type 42 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set