Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
297280011 | Benign myoclonic epilepsy in infancy | en | Synonym | Active | Case insensitive | SNOMED CT core |
297281010 | Neonatal myoclonic epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
576829014 | Benign myoclonic epilepsy in infancy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Benign myoclonic epilepsy in infancy | Is a | Idiopathic generalised epilepsy | true | Inferred relationship | Some | ||
Benign myoclonic epilepsy in infancy | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
Benign myoclonic epilepsy in infancy | Finding site | Structure of cerebrum | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
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