Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701667012 | Benign occipital epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3701669010 | Benign occipital lobe epilepsy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3701670011 | Benign occipital lobe epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3701668019 | A rare genetic neurological disorder with characteristics of visual seizures and occipital epileptiform paroxysms reactive to ocular opening which present in infancy to mid-adolescence. Vomiting, tonic eye deviation and impairment of consciousness are typically associated with the Panayiotopoulos type, while visual hallucinations, ictal blindness and post-ictal headache are commonly observed in the Gastaut type. Electroencephalographic findings in both types are similar and include bilateral, synchronous, high voltage spike-wave complexes in a normal background activity located predominantly in the occipital lobes. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Benign occipital lobe epilepsy | Finding site | Occipital lobe structure | true | Inferred relationship | Some | 1 | |
| Benign occipital lobe epilepsy | Is a | Occipital lobe epilepsy | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Benign occipital epilepsy of childhood - early onset variant | Is a | True | Benign occipital lobe epilepsy | Inferred relationship | Some | |
| Benign occipital epilepsy of childhood - late onset variant | Is a | True | Benign occipital lobe epilepsy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Queensland allied health indicator for intervention reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR