Status: retired, 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 |
119333016 | Symptomatic generalized epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
501972012 | Symptomatic generalised epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
501973019 | Secondary generalized epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
501974013 | Secondary generalised epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
812041018 | Symptomatic generalized epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Symptomatic generalized epilepsy | Is a | Generalized epilepsy | false | Inferred relationship | Some | ||
Symptomatic generalized epilepsy | Is a | Tonic-clonic epilepsy | false | Inferred relationship | Some | ||
Symptomatic generalized epilepsy | Finding site | Cerebrum | false | Inferred relationship | Some | 1 | |
Symptomatic generalized epilepsy | Has definitional manifestation | Seizure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Early infantile epileptic encephalopathy with suppression bursts | Is a | False | Symptomatic generalized epilepsy | Inferred relationship | Some | |
Symptomatic myoclonic epilepsy | Is a | False | Symptomatic generalized epilepsy | Inferred relationship | Some | |
Myoclonic encephalopathy | Is a | False | Symptomatic generalized epilepsy | Inferred relationship | Some | |
Pitt-Hopkins syndrome | Has definitional manifestation | False | Symptomatic generalized epilepsy | Inferred relationship | Some | |
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation | Is a | False | Symptomatic generalized epilepsy | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
REPLACED BY association reference set (foundation metadata concept)