Status: current, Primitive. Date: 31-Jul 2006. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
345311015 | Severe myoclonic epilepsy in infancy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3513043019 | Dravet Syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
618244013 | Severe myoclonic epilepsy in infancy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3513044013 | A genetic epilepsy of childhood with characteristics of drug-resistant seizures often induced by fever, presenting in previously healthy children, and which frequently leads to cognitive and motor impairment. Seizures can regress in adulthood but most patients have ongoing seizures that are refractory to medication. Around 85% of cases are due to a mutation or deletion in the SCN1A gene (2q24.3), encoding a voltage-gated sodium channel essential for the excitability of neurons. In families with a known SCN1A mutation, inheritance is autosomal dominant. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Severe myoclonic epilepsy in infancy | Interprets | Movement | false | Inferred relationship | Some | 2 | |
Severe myoclonic epilepsy in infancy | Is a | Myoclonic epilepsy of early childhood | false | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Occurrence | Childhood | false | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Occurrence | Infancy | false | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Is a | Epilepsy undetermined whether focal or generalised | false | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Severity | Severe | false | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Finding site | Structure of cerebrum | false | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Is a | Refractory myoclonic epilepsy | true | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Is a | Epileptic encephalopathy | true | Inferred relationship | Some | ||
Severe myoclonic epilepsy in infancy | Occurrence | Infancy | true | Inferred relationship | Some | 1 | |
Severe 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