OMOP Concept 4043550
Severe myoclonic epilepsy in infancy
StandardConditionSNOMED230437002Disorder
Maps from
8
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
8 source codes normalize to Severe myoclonic epilepsy in infancy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 126605 | Severe myoclonic epilepsy in infancy | Non-standard |
| ICD10CM | G40.83 | Dravet syndrome | Non-standard |
| ICD10CM | G40.833 | Dravet syndrome, intractable, with status epilepticus | Non-standard |
| ICD10CM | G40.834 | Dravet syndrome, intractable, without status epilepticus | Non-standard |
| Nebraska Lexicon | 230437002 | Dravet Syndrome | Non-standard |
| Nebraska Lexicon | 432161000124109 | Severe myoclonic epilepsy in infancy, non-intractable | Non-standard |
| Read | F25G.00 | Severe myoclonic epilepsy in infancy | Non-standard |
| Read | F25G.11 | Dravet syndrome | Non-standard |
Synonyms
Alternative names recorded for Severe myoclonic epilepsy in infancy across source vocabularies.
- Dravet Syndrome
- epilepsia mioclónica severa infantil
- epilepsia mioclónica severa infantil (trastorno)
- Severe myoclonic epilepsy in infancy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Developmental and epileptic encephalopathy
- 2Epilepsy
- 2Neurodevelopmental disorder
- 3Developmental disorder
- 3OMOP Seizure 1
- 3Seizure disorder
- 4Disease
- 4Disorder of brain
- 4Seizure
- 5Clinical finding
- 5Disorder of head
- 5Disorder of the central nervous system
- 5Finding of brain
- 5Seizure related finding
- 6Central nervous system finding
- 6Disorder of nervous system
- 6Head finding
- 6Neurological finding
- 7Disorder of body system
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