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 |
| 345236012 | Benign occipital epilepsy of childhood - early onset variant | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 618187017 | Benign occipital epilepsy of childhood - early onset variant (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2793363010 | Panayiotopoulos syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3701676017 | Benign childhood occipital epilepsy Panayiotopoulos type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3701677014 | Early-onset benign childhood occipital epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3701674019 | A rare genetic neurological disorder characterised by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalised convulsion. Autonomic status epilepticus may be the only clinical event in some cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3701675018 | A rare genetic neurological disorder characterized by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalized convulsion. Autonomic status epilepticus may be the only clinical event in some cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 811861000241118 | crise convulsive inaugurale de type Panayiotopoulos | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 832651000241117 | épilepsie occipitale bénigne précoce de l'enfance | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 832671000241110 | syndrome de Panayiotopoulos | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 839211000241112 | épilepsie occipitale bénigne à début précoce chez l'enfant | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Benign occipital epilepsy of childhood - early onset variant | Is a | Childhood epilepsy with occipital paroxysms | true | Inferred relationship | Some | ||
| Benign occipital epilepsy of childhood - early onset variant | Finding site | Occipital lobe structure | false | Inferred relationship | Some | ||
| Benign occipital epilepsy of childhood - early onset variant | Has definitional manifestation | Partial seizure | false | Inferred relationship | Some | ||
| Benign occipital epilepsy of childhood - early onset variant | Occurrence | Childhood | false | Inferred relationship | Some | ||
| Benign occipital epilepsy of childhood - early onset variant | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
| Benign occipital epilepsy of childhood - early onset variant | Is a | Benign occipital lobe epilepsy (disorder) | true | Inferred relationship | Some | ||
| Benign occipital epilepsy of childhood - early onset variant | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
| Benign occipital epilepsy of childhood - early onset variant | Finding site | Occipital lobe structure | true | Inferred relationship | Some | 1 | |
| Benign occipital epilepsy of childhood - early onset variant | Is a | Childhood seizure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR