Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3760106019 | Familial temporal lobe epilepsy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3760107011 | Familial temporal lobe epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3760108018 | Rare genetic epilepsy with characteristics of mostly benign simple or complex partial seizures with autonomic or psychic auras. Seizures occur infrequently, are of short duration and are usually well controlled with medication. Development and cognition are normal. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial temporal lobe epilepsy | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial temporal lobe epilepsy | Is a | Genetic disease | true | Inferred relationship | Some | ||
| Familial temporal lobe epilepsy | Is a | Temporal lobe epilepsy | true | Inferred relationship | Some | ||
| Familial 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
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR