Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3700714010 | Benign familial mesial temporal lobe epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3700715011 | Benign FMTLE (familial mesial temporal lobe epilepsy) | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3700716012 | Benign familial mesial temporal lobe epilepsy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3700717015 | Rare epilepsy with characteristics of seizures with viscerosensory or experiential auras, onset in adolescence or early adulthood and good prognosis. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Benign familial mesial temporal lobe epilepsy | Is a | Temporal lobe epilepsy | true | Inferred relationship | Some | ||
Benign familial mesial temporal lobe epilepsy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Benign familial mesial temporal lobe epilepsy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Benign familial mesial temporal lobe epilepsy | Finding site | Temporal lobe structure | 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
Description inactivation indicator reference set