OMOP Concept 4043411
Self-limited familial neonatal epilepsy
StandardConditionSNOMED230410004Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Self-limited familial neonatal epilepsy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 161092 | Benign familial neonatal seizures | Non-standard |
| CIEL | 161101 | Benign neonatal familial convulsions | Non-standard |
| Nebraska Lexicon | 230410004 | Benign familial infantile convulsions | Non-standard |
| Nebraska Lexicon | 279953009 | Familial neonatal seizures | Non-standard |
Synonyms
Alternative names recorded for Self-limited familial neonatal epilepsy across source vocabularies.
- Benign neonatal familial convulsions
- convulsiones neonatales familiares benignas
- epilepsia neonatal benigna
- epilepsia neonatal familiar autolimitada
- epilepsia neonatal familiar autolimitada (trastorno)
- Self-limited familial neonatal epilepsy (disorder)
- SeLFNE - self-limited familial neonatal epilepsy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Hereditary disorder of nervous system
- 1Self-limited neonatal epilepsy
- 2Autosomal hereditary disorder
- 2Disorder of nervous system
- 2Hereditary disorder by system
- 2Neonatal disorder
- 2Self-limited focal epilepsy
- 3Disorder of body system
- 3Disorder of fetus and/or newborn
- 3Finding of neonate
- 3Focal epilepsy
- 3Hereditary disease
- 4Clinical finding
- 4Disease
- 4Epilepsy
- 4Genetic disease
- 4OMOP Seizure 1
- 5Seizure disorder
- 6Disorder of brain
- 6Seizure
- 7Disorder of head
- 7Disorder of the central nervous system
- 7Finding of brain
- 7Seizure related finding
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