Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2967755016 | Hereditary essential tremor | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2967770015 | Hereditary essential tremor (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary essential tremor | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Hereditary essential tremor | Interprets | Movement | true | Inferred relationship | Some | 2 | |
| Hereditary essential tremor | Is a | Essential tremor | true | Inferred relationship | Some | ||
| Hereditary essential tremor | Finding site | Structure of nervous system | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Tremor, nystagmus, duodenal ulcer syndrome | Is a | True | Hereditary essential tremor | Inferred relationship | Some | |
| Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behaviour syndrome | Is a | True | Hereditary essential tremor | Inferred relationship | Some | |
| Sensorineural hearing loss, early greying, essential tremor syndrome | Is a | True | Hereditary essential tremor | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR