OMOP Concept 37168142
Developmental and epileptic encephalopathy
StandardConditionSNOMED1275631007Disorder
Maps from
4
Descendants
40
Valid from
31 May 2023
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Developmental and epileptic encephalopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133554 | Myoclonic encephalopathy | Non-standard |
| ICD10CM | G93.45 | Developmental and epileptic encephalopathy | Non-standard |
| MeSH | C562695 | Epileptic Encephalopathy, Early Infantile, 3 | Non-standard |
| Read | F132200 | Myoclonic encephalopathy | Non-standard |
Synonyms
Alternative names recorded for Developmental and epileptic encephalopathy across source vocabularies.
- DEE - developmental and epileptic encephalopathy
- Developmental and epileptic encephalopathy (disorder)
- encefalopatía epiléptica y de desarrollo
- encefalopatía epiléptica y de desarrollo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Epilepsy
- 1Neurodevelopmental disorder
- 2Developmental disorder
- 2OMOP Seizure 1
- 2Seizure disorder
- 3Disease
- 3Disorder of brain
- 3Seizure
- 4Clinical finding
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
- 4Seizure related finding
- 5Central nervous system finding
- 5Disorder of nervous system
- 5Head finding
- 5Neurological finding
- 6Disorder of body system
Narrower concepts
(40)Included automatically when you query with descendants.
- 1CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
- 1CDKL5 developmental and epileptic encephalopathy
- 1CNTNAP2-related developmental and epileptic encephalopathy
- 1Combined oxidative phosphorylation defect type 27
- 1Developmental and epileptic encephalopathy with spike-and-wave activation in sleep
- 1Dravet syndrome
- 1Early infantile developmental and epileptic encephalopathy
- 1Early-infantile developmental and epileptic encephalopathy
- 1Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome
- 1Epilepsy of infancy with migrating focal seizures
- 1Epilepsy with continuous spike wave during slow-wave sleep
- 1Epilepsy with myoclonic-atonic seizures
- 1Epileptic encephalopathy with global cerebral demyelination
- 1FASTKD2-related infantile mitochondrial encephalomyopathy
- 1Gelastic seizures with hypothalamic hamartoma
- 1GRIN2A developmental and epileptic encephalopathy
- 1Hyperekplexia epilepsy syndrome
- 1Infantile epileptic dyskinetic encephalopathy
- 1Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
- 1KCNQ2 developmental and epileptic encephalopathy
- 1Lennox-Gastaut syndrome
- 1Lethal neonatal spasticity, epileptic encephalopathy syndrome
- 1Multiple congenital anomalies, hypotonia, seizures syndrome type 2
- 1Multiple mitochondrial dysfunctions syndrome type 2
- 1Myoclonic epilepsy in non-progressive encephalopathy
Showing 25 of 40. Retrieve the full set via the API.
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