Status: current, Primitive. Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4964978016 | Spinocerebellar ataxia type 41 | en | Synonym | Active | Case insensitive | SNOMED CT core |
4964979012 | Spinocerebellar ataxia type 41 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4964980010 | A rare autosomal dominant cerebellar ataxia type III disorder with characteristics of adult-onset progressive imbalance and loss of coordination associated with an ataxic gait. Mild atrophy of the cerebellar vermis has been reported on brain magnetic resonance imaging. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Spinocerebellar ataxia type 41 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Spinocerebellar ataxia type 41 | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Spinocerebellar ataxia type 41 | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Spinocerebellar ataxia type 41 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Spinocerebellar ataxia type 41 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Spinocerebellar ataxia type 41 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 | |
Spinocerebellar ataxia type 41 | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Spinocerebellar ataxia type 41 | Clinical course | Progressive | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set