OMOP Concept 37205088
Familial epilepsy with auditory features
StandardConditionSNOMED784377008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Familial epilepsy with auditory features via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537297 | Autosomal Dominant Lateral Temporal Lobe Epilepsy | Non-standard |
Synonyms
Alternative names recorded for Familial epilepsy with auditory features across source vocabularies.
- Autosomal dominant epilepsy with auditory features
- Autosomal dominant lateral temporal lobe epilepsy
- epilepsia autosómica dominante con características auditivas
- epilepsia familiar con características auditivas
- epilepsia familiar con características auditivas (trastorno)
- Familial epilepsy with auditory features (disorder)
- FEAF - familial epilepsy with auditory features
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Epilepsy with auditory features
- 1Familial temporal lobe epilepsy
- 1Hereditary disorder of nervous system
- 2Autosomal hereditary disorder
- 2Disorder of nervous system
- 2Familial disease
- 2Genetic disease
- 2Hereditary disorder by system
- 2Lateral temporal lobe epilepsy
- 2Temporal lobe epilepsy
- 3Disease
- 3Disorder of body system
- 3Finding of head region
- 3Focal epilepsy
- 3Hereditary disease
- 4Clinical finding
- 4Epilepsy
- 4Head finding
- 4OMOP Seizure 1
- 5Seizure disorder
- 6Disorder of brain
- 6Seizure
- 7Disorder of head
- 7Disorder of the central nervous system
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