Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3700714010 | Benign familial mesial temporal lobe epilepsy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3700715011 | Benign FMTLE (familial mesial temporal lobe epilepsy) | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3700716012 | Benign familial mesial temporal lobe epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Benign familial mesial temporal lobe epilepsy | Is a | Temporal lobe epilepsy | true | Inferred relationship | Existential restriction modifier | ||
| Benign familial mesial temporal lobe epilepsy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Benign familial mesial temporal lobe epilepsy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Benign familial mesial temporal lobe epilepsy | Finding site | Temporal lobe structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR