OMOP Concept 35608023
Familial focal epilepsy with variable foci
StandardConditionSNOMED764522009Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Familial focal epilepsy with variable foci via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CN | G40.101 | Familial focal epilepsy (machine translation) | Non-standard |
| MeSH | C565785 | Epilepsy, Partial, with Variable Foci | Non-standard |
Synonyms
Alternative names recorded for Familial focal epilepsy with variable foci across source vocabularies.
- epilepsia focal familiar con focos variables
- epilepsia focal familiar con focos variables (trastorno)
- Familial focal epilepsy with variable foci (disorder)
- Familial partial epilepsy with variable foci
- FFEVF - familial focal epilepsy with variable foci
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Focal epilepsy
- 1Hereditary disorder of nervous system
- 2Autosomal hereditary disorder
- 2Disorder of nervous system
- 2Epilepsy
- 2Hereditary disorder by system
- 2OMOP Seizure 1
- 3Disorder of body system
- 3Hereditary disease
- 3Seizure disorder
- 4Disease
- 4Disorder of brain
- 4Genetic disease
- 4Seizure
- 5Clinical finding
- 5Disorder of head
- 5Disorder of the central nervous system
- 5Finding of brain
- 5Seizure related finding
- 6Central nervous system finding
- 6Head finding
- 6Neurological finding
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