Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701671010 | Benign childhood occipital epilepsy, Gastaut type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5382449016 | COVE - childhood occipital visual epilepsy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5382450016 | Late onset occipital epilepsy of childhood | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5382451017 | Childhood occipital visual epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5382452012 | Occipital epilepsy of childhood, Gastaut type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5382453019 | Childhood occipital visual epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3701672015 | A rare genetic neurological disorder with characteristics of childhood to mid-adolescence onset of frequent, brief, diurnal simple partial seizures which usually begin with visual hallucinations (e.g. phosphenes) and/or ictal blindness and may associate non visual seizures (such as deviation of the eyes, oculo clonic seizures), forced eyelid closure and blinking and sensory hallucinations. Post-ictal headache is common while impairment of consciousness is rare. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Childhood occipital visual epilepsy (disorder) | Is a | Childhood epilepsy with occipital paroxysms | false | Inferred relationship | Some | ||
| Childhood occipital visual epilepsy (disorder) | Has definitional manifestation | Partial seizure | false | Inferred relationship | Some | ||
| Childhood occipital visual epilepsy (disorder) | Finding site | Occipital lobe structure | false | Inferred relationship | Some | ||
| Childhood occipital visual epilepsy (disorder) | Occurrence | Childhood | false | Inferred relationship | Some | ||
| Childhood occipital visual epilepsy (disorder) | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
| Childhood occipital visual epilepsy (disorder) | Finding site | Occipital lobe structure | true | Inferred relationship | Some | 1 | |
| Childhood occipital visual epilepsy (disorder) | Is a | Childhood seizure | false | Inferred relationship | Some | ||
| Childhood occipital visual epilepsy (disorder) | Is a | Benign occipital lobe epilepsy (disorder) | true | Inferred relationship | Some | ||
| Childhood occipital visual epilepsy (disorder) | Occurrence | Childhood | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Benign occipital epilepsy of childhood - late onset, refractory | Is a | False | Childhood occipital visual epilepsy (disorder) | Inferred relationship | Some | |
| Benign occipital epilepsy of childhood - late onset, non-refractory | Is a | False | Childhood occipital visual epilepsy (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR