OMOP Concept 380378
Epilepsy
StandardConditionSNOMED84757009Disorder
Maps from
85
Descendants
217
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
85 source codes normalize to Epilepsy via the OMOP "Maps to" relationship.
Showing 25 of 85 source codes. Retrieve the full set via the API.
Synonyms
Alternative names recorded for Epilepsy across source vocabularies.
- epilepsia
- epilepsia (trastorno)
- Epilepsy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
Narrower concepts
(217)Included automatically when you query with descendants.
- 1Acquired epileptic aphasia, refractory
- 1Acute encephalopathy with biphasic seizures and late reduced diffusion
- 1Alopecia, epilepsy, intellectual disability syndrome Moynahan type
- 1Amelocerebrohypohidrotic syndrome
- 1Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
- 1Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
- 1Autism spectrum disorder, epilepsy, arthrogryposis syndrome
- 1Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
- 1Benign infantile focal epilepsy with midline spikes and waves during sleep
- 1Benign infantile seizure with mild gastroenteritis syndrome
- 1Celiac disease with epilepsy and cerebral calcification syndrome
- 1Combined focal and generalized epilepsy
- 1Congenital muscular dystrophy with intellectual disability and severe epilepsy
- 1Cryptogenic late-onset epileptic spasms
- 1DEND syndrome
- 1Developmental and epileptic encephalopathy
- 1Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
- 1Drug-induced epilepsy
- 1Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome
- 1Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome
- 1Epilepsy co-occurrent and due to degenerative brain disorder
- 1Epilepsy co-occurrent and due to dementia
- 1Epilepsy co-occurrent and due to demyelinating disorder
- 1Epilepsy co-occurrent and due to mesial temporal sclerosis
- 1Epilepsy due to bacterial endocarditis
Showing 25 of 217. Retrieve the full set via the API.
Get this concept via the API
Resolve Epilepsy - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/380378?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card