Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 345238013 | Primary inherited reading epilepsy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 618190011 | Primary inherited reading epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary inherited reading epilepsy | Is a | Localization-related idiopathic epilepsy | false | Inferred relationship | Existential restriction modifier | ||
| Primary inherited reading epilepsy | Finding site | Structure of cerebrum | true | Inferred relationship | Existential restriction modifier | 1 | |
| Primary inherited reading epilepsy | Has definitional manifestation | Seizure | false | Inferred relationship | Existential restriction modifier | ||
| Primary inherited reading epilepsy | Is a | Reflex epilepsy | true | Inferred relationship | Existential restriction modifier | ||
| Primary inherited reading epilepsy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR