Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4634546010 | Childhood-onset benign chorea with striatal involvement | en | Synonym | Active | Case insensitive | SNOMED CT core |
4634547018 | Childhood-onset benign chorea with striatal involvement (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4634548011 | A rare genetic hyperkinetic movement disorder with predominant characteristics of chorea of variable severity associated with bilateral striatal abnormalities on cerebral MRI. The disease is not progressive and cognitive performance is preserved in the majority of cases, although mild cognitive delay has also been reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Childhood-onset benign chorea with striatal involvement | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Childhood-onset benign chorea with striatal involvement | Is a | Benign hereditary chorea | true | Inferred relationship | Some | ||
Childhood-onset benign chorea with striatal involvement | Is a | Disorder of basal ganglia | true | Inferred relationship | Some | ||
Childhood-onset benign chorea with striatal involvement | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
Childhood-onset benign chorea with striatal involvement | Finding site | Corpus striatum structure | true | Inferred relationship | Some | 1 | |
Childhood-onset benign chorea with striatal involvement | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set