Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3637942018 | Ouvrier Billson syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3637943011 | Benign paroxysmal tonic upgaze of childhood with ataxia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3637944017 | Benign paroxysmal tonic upgaze of childhood with ataxia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3637945016 | A rare paroxysmal movement disorder with episodes of sustained, conjugate, upward deviation of the eyes and down beating saccades in attempted downgaze (with preserved horizontal eye movements). This is accompanied by ataxic symptoms (unsteady gait, lack of balance and movement coordination disturbances) in an otherwise healthy individual. Bilateral vertical nystagmus is associated. Symptoms generally disappear spontaneously within 1-2 years after onset. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Benign paroxysmal tonic upgaze of childhood with ataxia | Interprets | Movement | true | Inferred relationship | Some | 2 | |
Benign paroxysmal tonic upgaze of childhood with ataxia | Is a | Neurological disorder | true | Inferred relationship | Some | ||
Benign paroxysmal tonic upgaze of childhood with ataxia | Is a | Movement disorder | true | Inferred relationship | Some | ||
Benign paroxysmal tonic upgaze of childhood with ataxia | Finding site | Structure of nervous system | 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
Description inactivation indicator reference set