Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3723490014 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3723491013 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 771371000241111 | épilepsie temporale mésiale infantile avec régression cognitive sévère (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 910201000172112 | épilepsie temporale mésiale infantile avec régression cognitive sévère | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3723492018 | A rare monogenic disease with infantile-onset pharmacoresistant focal seizures of mesial temporal lobe onset manifesting with unresponsiveness, hypertonia and automatisms and cognitive regression soon after seizure onset leading to severe intellectual disability with behavioural abnormalities. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3723493011 | A rare monogenic disease with infantile-onset pharmacoresistant focal seizures of mesial temporal lobe onset manifesting with unresponsiveness, hypertonia and automatisms and cognitive regression soon after seizure onset leading to severe intellectual disability with behavioral abnormalities. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | survenue (attribut) | Infancy (qualifier value) | true | Inferred relationship | Some | 1 | |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | localisation d'une constatation (attribut) | Temporal lobe structure | true | Inferred relationship | Some | 1 | |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | est un(e) (attribut) | Temporal lobe epilepsy | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR