Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3313738013 | Episodic ataxia type 6 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3313739017 | Episodic ataxia type 6 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3313740015 | An exceedingly rare form of hereditary episodic ataxia with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Episodic ataxia type 6 | Is a | Episodic ataxia | true | Inferred relationship | Some | ||
Episodic ataxia type 6 | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Episodic ataxia type 6 | Is a | Cerebellar ataxia | true | Inferred relationship | Some | ||
Episodic ataxia type 6 | Is a | Hereditary disorder of nervous system | 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