Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 119333016 | Symptomatic generalized epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 119334010 | Symptomatic generalized epilepsy, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 501972012 | Symptomatic generalised epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501973019 | Secondary generalized epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 501974013 | Secondary generalised epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 812041018 | Symptomatic generalized epilepsy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Symptomatic generalised epilepsy | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
| Symptomatic generalised epilepsy | Is a | Generalised epilepsy | true | Inferred relationship | Some | ||
| Symptomatic generalised epilepsy | Is a | Tonic-clonic epilepsy | true | Inferred relationship | Some | ||
| Symptomatic generalised epilepsy | Finding site | Structure of cerebrum | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Myoclonic encephalopathy | Is a | True | Symptomatic generalised epilepsy | Inferred relationship | Some | |
| Early infantile epileptic encephalopathy with suppression bursts | Is a | True | Symptomatic generalised epilepsy | Inferred relationship | Some | |
| Symptomatic myoclonic epilepsy | Is a | True | Symptomatic generalised epilepsy | Inferred relationship | Some | |
| Pitt-Hopkins syndrome | Has definitional manifestation | False | Symptomatic generalised epilepsy | Inferred relationship | Some | |
| Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A (glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A) mutation | Is a | True | Symptomatic generalised 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