Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2023. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5160352010 | Genetic generalised epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5160353017 | GGE - genetic generalised epilepsy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5160355012 | Genetic generalized epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5160356013 | Genetic generalized epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5160358014 | GGE - genetic generalized epilepsy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5160354011 | Epilepsy with only generalised onset epileptic seizures and generalised spike-wave, due to a genetic or presumed genetic aetiology. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5160357016 | Epilepsy with only generalized onset epileptic seizures and generalized spike-wave, due to a genetic or presumed genetic etiology. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Genetic generalised epilepsy | Is a | Generalized epilepsy | true | Inferred relationship | Some | ||
| Genetic generalised epilepsy | Finding site | Brain structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Idiopathic generalized epilepsy | Is a | True | Genetic generalised epilepsy | Inferred relationship | Some | |
| Myoclonic epilepsy in infancy | Is a | True | Genetic generalised epilepsy | Inferred relationship | Some | |
| Epilepsy with eyelid myoclonia (disorder) | Is a | True | Genetic generalised epilepsy | Inferred relationship | Some | |
| Epilepsy with myoclonic absence (disorder) | Is a | True | Genetic generalised epilepsy | Inferred relationship | Some | |
| Epilepsy with myoclonic-atonic seizures (disorder) | Is a | True | Genetic generalised epilepsy | Inferred relationship | Some | |
| Perioral myoclonia with absences (disorder) | Is a | True | Genetic generalised epilepsy | Inferred relationship | Some |
This concept is not in any reference sets
FHIR