C06005
Data collected date and time
Date (and time, if applicable and known) the data were collected. This may be the date/time a particular examination or procedure was performed.
Supplemental-Highly Recommended
Classification of Seizures
False
Epilepsy
Epilepsy
C14134
Data valid through date and time
Date (and time, if applicable and known) the data collected are valid through
Supplemental-Highly Recommended
Classification of Seizures
False
Epilepsy
Epilepsy
C58583
Seizure epilepsy focal classification type
The type of focal epileptic seizures, considered to originate within networks limited to one hemisphere, which may be discretely localized or more widely distributed, and may originate in subcortical structures, experience by the participant/subject.
Supplemental-Highly Recommended
Classification of Seizures
False
Epilepsy
Epilepsy
C58599
Seizure epilepsy generalized classification type
The type of generalized epileptic seizures, considered to originate at some point within, and rapidly engage, bilaterally distributed networks and may include such bilateral networks as cortical and subcortical structures, but do not necessarily include the entire cortex, experienced by the participant/subject.
Supplemental-Highly Recommended
Classification of Seizures
False
Epilepsy
Epilepsy
C58604
Seizure unclassified classification status
The element related to the degree to which unclassified seizures are present
Supplemental-Highly Recommended
Classification of Seizures
False
Epilepsy
Epilepsy
C14425
Epilepsy etiology specific attribution confidence type
The level of confidence attributed to the categorizing of specific etiology of epilepsy to genetic or presumed genetic, structural, metabolic, immune, infectious or unknown factors.
Supplemental-Highly Recommended
Classification of Etiology
False
Epilepsy
Epilepsy
C14426
Epilepsy etiology primary type
Primary etiologic cause for epilepsy when multiple etiologies are present (i.e., more than one etiology, as described by the International League Against Epilepsy, is coded as definite or possible).
Supplemental-Highly Recommended
Classification of Etiology
False
Epilepsy
Epilepsy
C14427
Epilepsy etiology secondary type
Secondary etiologic cause for epilepsy when multiple etiologies are present (i.e., more than one etiology, as described by the International League Against Epilepsy, is coded as definite or possible).
Supplemental-Highly Recommended
Classification of Etiology
False
Epilepsy
Epilepsy
C58582
Genetic presumed genetic epilepsy etiology type
The categorization for genetic or presumed genetic etiology of epilepsy
Supplemental-Highly Recommended
Classification of Etiology
False
Epilepsy
Epilepsy
C58587
Structural epilepsy etiology type
The categorization for structural etiology of epilepsy
Supplemental-Highly Recommended
Classification of Etiology
False
Epilepsy
Epilepsy
C58605
Metabolic toxic epilepsy etiology type
The categorization for metabolic toxic etiology of epilepsy
Supplemental-Highly Recommended
Classification of Etiology
False
Epilepsy
Epilepsy
C58606
Other epilepsy etiology type
The categorization for other etiology of epilepsy
Supplemental-Highly Recommended
Classification of Etiology
False
Epilepsy
Epilepsy
C06005
Data collected date and time
Date (and time, if applicable and known) the data were collected. This may be the date/time a particular examination or procedure was performed.
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14134
Data valid through date and time
Date (and time, if applicable and known) the data collected are valid through
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14470
Epilepsy syndrome likelihood present type
Certainty of whether the participant/subject has or had the epilepsy syndrome for the particular age period
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14471
Epilepsy syndrome neonatal onset type
Common epilepsy syndromes with onset in the neonatal period (
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14472
Epilepsy syndrome age of onset type
Age period during which the epilepsy syndrome first appeared
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14473
Epilepsy syndrome infant onset type
Common epilepsy syndromes for infants, children less than 2 years of age.
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14475
Epilepsy syndrome childhood onset type
Common epilepsy syndromes for children, 2-12 years of age.
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14477
Epilepsy syndrome adolescence adult onset type
Common epilepsy syndromes for adolescents, children 12-18 years of age, and adults, person older than 18 years of age.
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14479
Epilepsy syndrome less specific age relationship type
Common epilepsy syndromes that have a less specific age or no association with a specific age on onset.
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14481
Epilepsy syndrome distinctive constellation type
Syndromes with distinctive constellations, diagnostically meaningful forms of epilepsy and may have implications for clinical treatment, particularly surgery.
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C14485
Epilepsy syndromes distinct confidence level type
Confidence level that the two or more epilepsy syndromes selected as present are distinct syndromes
Supplemental-Highly Recommended
Syndromes by Age of Onset
False
Epilepsy
Epilepsy
C10626
Condition diary date and time
Date (and time, if applicable and known) the diary data are recorded
Supplemental-Highly Recommended
Seizure Diary
False
Epilepsy
Epilepsy
C10635
Seizure daily diary seizure type
Type of seizure experienced by the participant/subject on the specific date
Supplemental-Highly Recommended
Seizure Diary
False
Epilepsy
Epilepsy