Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 119333016 | Symptomatic generalized epilepsy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 501972012 | Symptomatic generalised epilepsy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 501973019 | Secondary generalized epilepsy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 501974013 | Secondary generalised epilepsy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 812041018 | Symptomatic generalized epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Symptomatic generalized epilepsy | Is a | Generalized epilepsy | true | Inferred relationship | Existential restriction modifier | ||
| Symptomatic generalized epilepsy | Is a | Tonic-clonic epilepsy | true | Inferred relationship | Existential restriction modifier | ||
| Symptomatic generalized epilepsy | Finding site | Structure of cerebrum | true | Inferred relationship | Existential restriction modifier | 1 | |
| Symptomatic generalized epilepsy | Has definitional manifestation | Seizure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Early infantile epileptic encephalopathy with suppression bursts | Is a | True | Symptomatic generalized epilepsy | Inferred relationship | Existential restriction modifier | |
| Symptomatic myoclonic epilepsy | Is a | True | Symptomatic generalized epilepsy | Inferred relationship | Existential restriction modifier | |
| Myoclonic encephalopathy | Is a | True | Symptomatic generalized epilepsy | Inferred relationship | Existential restriction modifier | |
| Pitt-Hopkins syndrome | Has definitional manifestation | False | Symptomatic generalized epilepsy | Inferred relationship | Existential restriction modifier | |
| Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation | Is a | True | Symptomatic generalized epilepsy | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR