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 |
| 3763854011 | Autosomal dominant epilepsy with auditory features | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763855012 | Autosomal dominant lateral temporal lobe epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5380923012 | Familial epilepsy with auditory features | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5380924018 | Familial epilepsy with auditory features (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5380925017 | FEAF - familial epilepsy with auditory features | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 8010841000146117 | autosomaal dominante epilepsie met auditieve verschijnselen (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8010851000146119 | autosomaal dominante epilepsie met auditieve verschijnselen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3763856013 | A rare genetic familial partial epilepsy disease with characteristics of focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial epilepsy with auditory features | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial epilepsy with auditory features | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Familial epilepsy with auditory features | Is a | Familial disease | false | Inferred relationship | Some | ||
| Familial epilepsy with auditory features | Is a | Temporal lobe epilepsy | false | Inferred relationship | Some | ||
| Familial epilepsy with auditory features | Finding site | Temporal lobe structure | true | Inferred relationship | Some | 1 | |
| Familial epilepsy with auditory features | Is a | Epilepsy with auditory features (disorder) | true | Inferred relationship | Some | ||
| Familial epilepsy with auditory features | Is a | Familial temporal lobe epilepsy (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR