Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2994998010 | Familial Pick's disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2995187016 | Frontotemporal dementia with parkinsonism-17 | en | Synonym | Active | Case insensitive | SNOMED CT core |
2995324015 | Wilhelmsen-Lynch disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
2995445011 | Disinhibition-dementia-parkinsonism-amytrophy complex | en | Synonym | Active | Case insensitive | SNOMED CT core |
2995675012 | Frontotemporal dementia with parkinsonism-17 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2995742010 | FTDP-17 - Frontotemporal dementia with parkinsonism 17 | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Frontotemporal dementia with parkinsonism-17 | Interprets | Movement | true | Inferred relationship | Some | 2 | |
Frontotemporal dementia with parkinsonism-17 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Frontotemporal dementia with parkinsonism-17 | Is a | Encephalopathy | true | Inferred relationship | Some | ||
Frontotemporal dementia with parkinsonism-17 | Is a | Movement disorder | true | Inferred relationship | Some | ||
Frontotemporal dementia with parkinsonism-17 | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Frontotemporal dementia with parkinsonism-17 | Finding site | Brain structure | true | 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