Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3763836012 | Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763837015 | Familial mesial temporal lobe epilepsy with febrile seizures | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763838013 | A rare genetic familial partial epilepsy disease with characteristics of simple partial seizures, complex partial seizures and/or secondarily generalized seizures, originating from the inner aspect of the temporal lobe, associated with an antecedent history of febrile seizures, occurring in various members of a family. Hippocampal abnormalities (for example hippocampal sclerosis) may also be associated. There is evidence the disease is caused by homozygous mutation in the CPA6 gene on chromosome 8q13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3763839017 | A rare genetic familial partial epilepsy disease with characteristics of simple partial seizures, complex partial seizures and/or secondarily generalised seizures, originating from the inner aspect of the temporal lobe, associated with an antecedent history of febrile seizures, occurring in various members of a family. Hippocampal abnormalities (for example hippocampal sclerosis) may also be associated. There is evidence the disease is caused by homozygous mutation in the CPA6 gene on chromosome 8q13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | est un(e) (attribut) | convulsion fébrile | false | Inferred relationship | Some | ||
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | est un(e) (attribut) | Familial disease | false | Inferred relationship | Some | ||
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | est un(e) (attribut) | trouble caractérisé par de la fièvre | false | Inferred relationship | Some | ||
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | est un(e) (attribut) | Temporal lobe epilepsy | true | Inferred relationship | Some | ||
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | associé à (attribut) | Fever | false | Inferred relationship | Some | 2 | |
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | localisation d'une constatation (attribut) | Temporal lobe structure | true | Inferred relationship | Some | 1 | |
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | est un(e) (attribut) | Familial febrile convulsions | true | Inferred relationship | Some | ||
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | interprète (attribut) | Body temperature (observable entity) | true | Inferred relationship | Some | 2 | |
| Familial mesial temporal lobe epilepsy with febrile seizures (disorder) | a pour interprétation (attribut) | au-dessus de l'étendue de référence | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR