Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Generalized convulsive epilepsy | est un(e) (attribut) | épilepsie tonicoclonique | true | Inferred relationship | Some | ||
Generalized convulsive epilepsy | est défini par la manifestation de (attribut) | convulsion | false | Inferred relationship | Some | ||
Generalized convulsive epilepsy | est un(e) (attribut) | Generalized epilepsy | true | Inferred relationship | Some | ||
Generalized convulsive epilepsy | localisation d'une constatation (attribut) | structure du cerveau | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
état de grand mal épileptique | est un(e) (attribut) | True | Generalized convulsive epilepsy | Inferred relationship | Some | |
Other specified generalized convulsive epilepsy | est un(e) (attribut) | False | Generalized convulsive epilepsy | Inferred relationship | Some | |
Generalized convulsive epilepsy NOS | est un(e) (attribut) | False | Generalized convulsive epilepsy | Inferred relationship | Some | |
Epilepsy with grand mal seizures on awakening | est un(e) (attribut) | True | Generalized convulsive epilepsy | Inferred relationship | Some | |
Refractory generalized convulsive epilepsy | est un(e) (attribut) | True | Generalized convulsive epilepsy | Inferred relationship | Some | |
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) | est un(e) (attribut) | True | Generalized convulsive epilepsy | Inferred relationship | Some |
Reference Sets