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 |
| 3723490014 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3723491013 | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression | Occurrence | Infancy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression | Finding site | Temporal lobe structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression | Is a | Temporal lobe epilepsy | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR