Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3650197015 | FFEVF - familial focal epilepsy with variable foci | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3650198013 | Familial focal epilepsy with variable foci | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3650199017 | Familial partial epilepsy with variable foci | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3650200019 | Familial focal epilepsy with variable foci (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial focal epilepsy with variable foci | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial focal epilepsy with variable foci | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Familial focal epilepsy with variable foci | Is a | Localization-related symptomatic epilepsy | true | Inferred relationship | Existential restriction modifier | ||
| Familial focal epilepsy with variable foci | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Familial focal epilepsy with variable foci | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial focal epilepsy with variable foci | Finding site | Structure of cerebrum | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR