Name Steward Organization Suggested Domain Suggested Domain Description Cde Group Classification
Epilepsy syndrome childhood onset type NINDS Disease characterization
Including Alzheimer's Disease (AD)/AD-Related Dementias (ADRD) diagnosis and multiple chronic conditions (MCCs)
NIH CDEs
  • NINDS
    • Disease
      • Epilepsy
        • Classification
          • Supplemental-Highly Recommended
        • Domain
          • Disease/Injury Related Events
            • Classification
    • Domain
      • Disease/Injury Related Events
        • Classification
    • Population
      • Adult
      • Pediatric

# Datatype
Value List

# Permissible value Value meaning name Value meaning definition
Autosomal-dominant nocturnal frontal lobe epilepsy Autosomal-dominant nocturnal frontal lobe epilepsy Autosomal-dominant nocturnal frontal lobe epilepsy (ADNFLE)
Benign childhood epilepsy with centrotemporal spikes Benign childhood epilepsy with centrotemporal spikes Benign childhood epilepsy with centrotemporal spikes (BCECTS)
Childhood absence epilepsy Childhood absence epilepsy Childhood absence epilepsy (CAE)
Early onset benign childhood occipital epilepsy Early onset benign childhood occipital epilepsy Early onset benign childhood occipital epilepsy (Panayiotopoulos type)
Epilepsy with myoclonic absences Epilepsy with myoclonic absences Epilepsy with myoclonic absences
Epilepsy with myoclonic atonic seizures Epilepsy with myoclonic atonic seizures Epilepsy with myoclonic atonic seizures
Epileptic encephalopathy with continuous spike-and-wave during sleep Epileptic encephalopathy with continuous spike-and-wave during sleep Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)
Febrile seizures plus Febrile seizures plus Febrile seizures plus (FS+, can start in infancy)
Landau-Kleffner syndrome Landau-Kleffner syndrome Landau-Kleffner syndrome (LKS)
Late onset childhood occipital epilepsy Late onset childhood occipital epilepsy Late onset childhood occipital epilepsy (Gastaut type)
Lennox-Gastaut syndrome Lennox-Gastaut syndrome Lennox-Gastaut syndrome
Other, specify Other, specify Other, specify

# Definition
Common epilepsy syndromes for children, 2-12 years of age.

# Designation
Epilepsy syndrome childhood onset type

# Identifier Origin Version
M188Y9KYvkV NLM CDEs 12-02-2025-download
EpilepsySyndChildOnsetTyp BRICS Variable Name N/A
C14475 NINDS 3