Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
293387010 | Westphal-Strumpell syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4572807010 | Westphal-Strumpell cerebral pseudosclerosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
4572808017 | Pseudosclerotic type of Wilson's disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
4572809013 | Westphal-Strumpell form of Wilson's disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
574452017 | Westphal-Strumpell syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Westphal-Strumpell syndrome | Finding site | Brain tissue structure | true | Inferred relationship | Some | 2 | |
Westphal-Strumpell syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Westphal-Strumpell syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 | |
Westphal-Strumpell syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 3 | |
Westphal-Strumpell syndrome | Finding site | Liver structure | true | Inferred relationship | Some | 1 | |
Westphal-Strumpell syndrome | Finding site | Body tissue structure | true | Inferred relationship | Some | 3 | |
Westphal-Strumpell syndrome | Is a | Wilson's disease | true | Inferred relationship | Some | ||
Westphal-Strumpell syndrome | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set