OMOP Concept 380378
Epilepsy
StandardConditionSNOMED84757009Disorder
Maps from
88
Descendants
224
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
88 source codes normalize to Epilepsy via the OMOP "Maps to" relationship.
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
(224)Included automatically when you query with descendants.
- 1Acquired epileptic aphasia
- 1Acute encephalopathy with biphasic seizures and late reduced diffusion
- 1Alopecia, epilepsy, intellectual disability syndrome Moynahan type
- 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 adult familial myoclonic epilepsy
- 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
- 1Cognitive dysfunction with epilepsy
- 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 complicating pregnancy
- 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
- 1Epilepsy due to cerebrovascular accident
- 1Epilepsy due to congenital anomaly of brain
- 1Epilepsy due to congenital infectious disease
- 1Epilepsy due to glucose transporter protein type 1 deficiency syndrome
- 1Epilepsy due to immune disorder
- 1Epilepsy due to infectious disease of central nervous system
- 1Epilepsy due to intracranial tumor
- 1Epilepsy due to parasitic disease
- 1Epilepsy due to perinatal anoxic-ischemic brain injury
- 1Epilepsy due to perinatal cerebral ischemia
- 1Epilepsy due to perinatal intraventricular hemorrhage
- 1Epilepsy due to perinatal periventricular hemorrhage
- 1Epilepsy due to Rasmussen syndrome
- 1Epilepsy in mother complicating childbirth
- 1Epilepsy in mother complicating pregnancy
- 1Epilepsy, microcephaly, skeletal dysplasia syndrome
- 1Epilepsy of infancy with migrating focal seizures
- 1Epilepsy telangiectasia syndrome
- 1Epileptic dementia with behavioral disturbance
- 1Epileptic encephalopathy
- 1Exacerbation of epilepsy
- 1Familial infantile myoclonic epilepsy
- 1Fatty acyl-CoA reductase 1 deficiency
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