ID

43611

Beschrijving

NINDS Common Data Elements Used from the National Institute of Neurological Disorders and Stroke Common Data Elements (https://www.commondataelements.ninds.nih.gov/) References: Grinnon ST, Miller K, Marler JR, Lu Y, Stout A, Odenkirchen J, Kunitz S. National Institute of Neurological Disorders and Stroke Common Data Element Project - approach and methods. Clin Trials. 2012;9(3):322-9.

Link

https://www.commondataelements.ninds.nih.gov/

Trefwoorden

  1. 19-04-16 19-04-16 -
  2. 20-09-21 20-09-21 -
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20 september 2021

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Licentie

Creative Commons BY-NC 3.0

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NINDS CDE Classification of Etiology,Seizures and syndromes by age of onset Epilepsy

Classification of Etiology,Seizures and syndromes by age of onset

Classification of Etiology
Beschrijving

Classification of Etiology

Genetic or presumed genetic OR epilepsy of unknown cause
Beschrijving

Etiology

Datatype

integer

Alias
UMLS CUI [1]
C2724370
Structural or metabolic
Beschrijving

Etiology

Datatype

integer

Alias
UMLS CUI [1]
C2724370
Specific Etiology
Beschrijving

Specific Etiology

Viral, bacterial and parasitic infections
Beschrijving

Infections

Datatype

integer

Alias
UMLS CUI [1]
C0009450
Viral, bacterial and parasitic infections
Beschrijving

Infections

Datatype

integer

Alias
UMLS CUI [1]
C0009450
Viral, bacterial and parasitic infections: If more than one specific etiology, please specify
Beschrijving

Infections

Datatype

text

Alias
UMLS CUI [1]
C0009450
Traumatic brain injury
Beschrijving

Traumatic brain injury

Datatype

integer

Alias
UMLS CUI [1]
C0876926
Traumatic brain injury
Beschrijving

Traumatic brain injury

Datatype

integer

Alias
UMLS CUI [1]
C0876926
Traumatic brain injury: If more than one specific etiology is selected, specify
Beschrijving

Traumatic brain injury

Datatype

text

Alias
UMLS CUI [1]
C0876926
Stroke
Beschrijving

Stroke

Datatype

integer

Alias
UMLS CUI [1]
C0038454
Stroke
Beschrijving

Stroke

Datatype

integer

Alias
UMLS CUI [1]
C0038454
Stroke: If more than one specific etiology is selected, specify:
Beschrijving

Stroke

Datatype

text

Alias
UMLS CUI [1]
C0038454
Intraventricular hemorrhage
Beschrijving

Intraventricular hemorrhage

Datatype

integer

Alias
UMLS CUI [1]
C0240059
Intraventricular hemorrhage
Beschrijving

Intraventricular hemorrhage

Datatype

integer

Alias
UMLS CUI [1]
C0240059
Intraventricular hemorrhage: If more than one specific etiology is selected, specify:
Beschrijving

Intraventricular hemorrhage

Datatype

text

Alias
UMLS CUI [1]
C0240059
Hypoxic-ischemic encephalopathy
Beschrijving

Hypoxic-ischemic encephalopathy

Datatype

integer

Alias
UMLS CUI [1]
C0149878
Hypoxic-ischemic encephalopathy
Beschrijving

Hypoxic-ischemic encephalopathy

Datatype

integer

Alias
UMLS CUI [1]
C0149878
Hypoxic-ischemic encephalopathy: If more than one specific etiology is selected, specify:
Beschrijving

Hypoxic-ischemic encephalopathy

Datatype

text

Alias
UMLS CUI [1]
C0149878
Other metabolic or toxic insults
Beschrijving

Other metabolic or toxic insults

Datatype

integer

Alias
UMLS CUI [1]
C0600688
UMLS CUI [2]
C0006112
Other metabolic or toxic insults
Beschrijving

Other metabolic or toxic insults

Datatype

integer

Alias
UMLS CUI [1]
C0600688
UMLS CUI [2]
C0006112
Other metabolic or toxic insults:If more than one specific etiology is selected, specify:
Beschrijving

Other metabolic or toxic insults

Datatype

text

Alias
UMLS CUI [1]
C0600688
UMLS CUI [2]
C0006112
Neurocutaneous syndromes
Beschrijving

Neurocutaneous syndromes

Datatype

integer

Alias
UMLS CUI [1]
C0265316
Neurocutaneous syndromes
Beschrijving

Neurocutaneous syndromes

Datatype

integer

Alias
UMLS CUI [1]
C0265316
Neurocutaneous syndromes: If more than one specific etiology is selected, specify:
Beschrijving

Neurocutaneous syndromes

Datatype

text

Alias
UMLS CUI [1]
C0265316
Inborn errors of metabolism
Beschrijving

Inborn errors of metabolism

Datatype

integer

Alias
UMLS CUI [1]
C0025521
Inborn errors of metabolism
Beschrijving

Inborn errors of metabolism

Datatype

integer

Alias
UMLS CUI [1]
C0025521
Inborn errors of metabolism:If more than one specific etiology is selected, specify:
Beschrijving

Inborn errors of metabolism

Datatype

text

Alias
UMLS CUI [1]
C0025521
Genetic and chromosomal development encephalopathies
Beschrijving

Genetic and chromosomal development encephalopathies

Datatype

integer

Alias
UMLS CUI [1,1]
C0085584
UMLS CUI [1,2]
C0008626
UMLS CUI [1,3]
C0314603
Genetic and chromosomal development encephalopathies
Beschrijving

Genetic and chromosomal development encephalopathies

Datatype

integer

Alias
UMLS CUI [1,1]
C0085584
UMLS CUI [1,2]
C0008626
UMLS CUI [1,3]
C0314603
Genetic and chromosomal development encephalopathies: If more than one specific etiology is selected, specify
Beschrijving

Genetic and chromosomal development encephalopathies

Datatype

text

Alias
UMLS CUI [1,1]
C0085584
UMLS CUI [1,2]
C0008626
UMLS CUI [1,3]
C0314603
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy
Beschrijving

Developmental encephalopathy of unknown cause

Datatype

integer

Alias
UMLS CUI [1,1]
C0085584
UMLS CUI [1,2]
C0458003
UMLS CUI [1,3]
C1385132
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy
Beschrijving

Developmental encephalopathy of unknown cause

Datatype

integer

Alias
UMLS CUI [1,1]
C0085584
UMLS CUI [1,2]
C0458003
UMLS CUI [1,3]
C1385132
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy: If more than one specific etiology is selected, specify
Beschrijving

Developmental encephalopathy of unknown cause

Datatype

text

Alias
UMLS CUI [1,1]
C0085584
UMLS CUI [1,2]
C0458003
UMLS CUI [1,3]
C1385132
Malformations of cortical or other brain development with or without known genetic determinants
Beschrijving

Malformations of cortical or other brain development

Datatype

integer

Alias
UMLS CUI [1]
C1955869
UMLS CUI [2]
C0266449
Malformations of cortical or other brain development with or without known genetic determinants
Beschrijving

Malformations of cortical or other brain development

Datatype

integer

Alias
UMLS CUI [1]
C1955869
UMLS CUI [2]
C0266449
Malformations of cortical or other brain development with or without known genetic determinants: If more than one specific etiology is selected, specify
Beschrijving

Malformations of cortical or other brain development

Datatype

text

Alias
UMLS CUI [1]
C1955869
UMLS CUI [2]
C0266449
Neoplasia
Beschrijving

Neoplasia

Datatype

integer

Alias
UMLS CUI [1]
C1882062
Neoplasia
Beschrijving

Neoplasia

Datatype

integer

Alias
UMLS CUI [1]
C1882062
Neoplasia: If more than one specific etiology is selected, specify
Beschrijving

Neoplasia

Datatype

text

Alias
UMLS CUI [1]
C1882062
Mesial temporal sclerosis
Beschrijving

Mesial temporal sclerosis

Datatype

integer

Alias
UMLS CUI [1]
C2062593
Mesial temporal sclerosis
Beschrijving

Mesial temporal sclerosis

Datatype

integer

Alias
UMLS CUI [1]
C2062593
Mesial temporal sclerosis: If more than one specific etiology is selected, specify
Beschrijving

Mesial temporal sclerosis

Datatype

text

Alias
UMLS CUI [1]
C2062593
Dementia
Beschrijving

Dementia

Datatype

integer

Alias
UMLS CUI [1]
C0497327
Dementia
Beschrijving

Dementia

Datatype

integer

Alias
UMLS CUI [1]
C0497327
Dementia: If more than one specific etiology is selected, specify
Beschrijving

Dementia

Datatype

text

Alias
UMLS CUI [1]
C0497327
Other degenerative neurologic diseases
Beschrijving

Degenerative neurologic diseases

Datatype

integer

Alias
UMLS CUI [1]
C0524851
Other degenerative neurologic diseases
Beschrijving

Degenerative neurologic diseases

Datatype

integer

Alias
UMLS CUI [1]
C0524851
Genetic or presumed genetic, if known specify:
Beschrijving

Genetic or presumed genetic

Datatype

text

Alias
UMLS CUI [1]
C0017399
Genetic or presumed genetic
Beschrijving

Genetic or presumed genetic

Datatype

integer

Alias
UMLS CUI [1]
C0017399
Genetic or presumed genetic
Beschrijving

Genetic or presumed genetic

Datatype

integer

Alias
UMLS CUI [1]
C0017399
Genetic or presumed genetic, if more than one specific etiology is selected, specify:
Beschrijving

Genetic or presumed genetic,

Datatype

text

Alias
UMLS CUI [1]
C0017399
Epilepsy of unknown cause, without relevant abnormalities on examination, cognition, history, or imaging
Beschrijving

Epilepsy of unknown cause

Datatype

integer

Alias
UMLS CUI [1]
C0086237
Epilepsy of unknown cause, without relevant abnormalities on examination, cognition, history, or imaging
Beschrijving

Epilepsy of unknown cause

Datatype

integer

Alias
UMLS CUI [1]
C0086237
Epilepsy of unknown cause without relevant abnormalities on examination, cognition, history, or imaging:If more than one specific etiology is selected, specify
Beschrijving

Epilepsy of unknown cause

Datatype

text

Alias
UMLS CUI [1]
C0086237
Other Etiology, specify:
Beschrijving

Other Etiology

Datatype

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0015127
Other etiology
Beschrijving

Other etiology

Datatype

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0015127
Other etiology
Beschrijving

Other etiology

Datatype

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0015127
Other etiology,If more than one specific etiology is selected, specify:
Beschrijving

Other etiology

Datatype

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0015127
Classification of Seizures
Beschrijving

Classification of Seizures

Generalized seizures
Beschrijving

Please complete table of Generalized seizure subtypes

Datatype

boolean

Alias
UMLS CUI [1]
C0234533
Tonic clonic seizures (in any combination)
Beschrijving

Generalized Seizure Tonic clonic

Datatype

integer

Alias
UMLS CUI [1]
C0748577
Absence
Beschrijving

Generalized Seizure Absence

Datatype

integer

Alias
UMLS CUI [1]
C0014553
Generalized Seizure Typical
Beschrijving

Generalized Seizure Typical

Datatype

integer

Alias
UMLS CUI [1]
C0311334
Generalized Seizure Atypical
Beschrijving

Generalized Seizure Atypical

Datatype

integer

Alias
UMLS CUI [1]
C0595948
Generalized Seizure Myoclonic absence
Beschrijving

Generalized Seizure Myoclonic absence

Datatype

integer

Alias
UMLS CUI [1]
C0393703
Generalized Seizure Eyelid myoclonia
Beschrijving

Generalized Seizure Eyelid myoclonia

Datatype

integer

Alias
UMLS CUI [1]
C4023513
Generalized Seizure Myoclonic
Beschrijving

Generalized Seizure Myoclonic

Datatype

integer

Alias
UMLS CUI [1]
C0014550
Generalized Seizure Myoclonic atonic
Beschrijving

Generalized Seizure Myoclonic atonic

Datatype

integer

Alias
UMLS CUI [1]
C0393702
Generalized Seizure Myoclonic tonic
Beschrijving

Generalized Seizure Myoclonic tonic

Datatype

integer

Alias
UMLS CUI [1,1]
C0014550
UMLS CUI [1,2]
C0270844
Generalized Seizure Clonic
Beschrijving

Generalized Seizure Clonic

Datatype

integer

Alias
UMLS CUI [1]
C0234535
Generalized seizures tonic
Beschrijving

Generalized seizures tonic

Datatype

integer

Alias
UMLS CUI [1]
C0270844
Generalized seizures atonic
Beschrijving

Generalized seizures atonic

Datatype

integer

Alias
UMLS CUI [1]
C2228222
Focal seizures
Beschrijving

Please complete table of Focal seizure subtypes

Datatype

boolean

Alias
UMLS CUI [1]
C0751495
Focal Seizure without impairment of consciousness or responsiveness
Beschrijving

Focal Seizure Subtypes (according to degree of impairment)

Datatype

integer

Alias
UMLS CUI [1]
C0751495
Focal Seizure with observable motor or autonomic components (roughly corresponds to the concept of “simple partial seizure”)
Beschrijving

Focal Seizure

Datatype

integer

Alias
UMLS CUI [1]
C0016399
Focal Seizure involving subjective sensory or psychic phenomena only (corresponds to the concept of “aura”)
Beschrijving

Focal Seizure

Datatype

integer

Alias
UMLS CUI [1]
C0752322
Focal Seizure with impairment of consciousness or responsiveness (roughly corresponds to the concept of “complex partial seizure”)
Beschrijving

Focal Seizure

Datatype

integer

Alias
UMLS CUI [1]
C0270834
Focal Seizure evolving to a bilateral, convulsive seizure (involving tonic, clonic, or tonic and clonic components; replaces the term “secondarily generalized seizure”)
Beschrijving

Focal Seizure

Datatype

integer

Alias
UMLS CUI [1]
C2875090
Unclassified Seizure
Beschrijving

Please complete table of Unclassified seizure type

Datatype

boolean

Alias
UMLS CUI [1]
C0270826
Unclassified Seizure Epileptic spasms – focal or generalized
Beschrijving

Unclassified Seizure

Datatype

integer

Alias
UMLS CUI [1]
C0270826
Unclassified Seizure
Beschrijving

Unclassified Seizure

Datatype

integer

Alias
UMLS CUI [1]
C0270826
If two or more seizure types were selected as present, rate the confidence level that these are distinct seizure types
Beschrijving

confidence level

Datatype

integer

Alias
UMLS CUI [1]
C0518578
Date of completion of this form
Beschrijving

Date of completion

Datatype

date

Alias
UMLS CUI [1]
C0011008
Information complete up to (mm/dd/yyyy)
Beschrijving

Information complete

Datatype

date

Alias
UMLS CUI [1,1]
C0205197
UMLS CUI [1,2]
C0012972
Syndromes by Age of Onset
Beschrijving

Syndromes by Age of Onset

Benign familial neonatal epilepsy (BFNE)
Beschrijving

Neonatal Period BFNE

Datatype

integer

Alias
UMLS CUI [1]
C0220669
Early myoclonic encephalopathy (EME)
Beschrijving

Neonatal Period EME

Datatype

integer

Alias
UMLS CUI [1]
C0270855
Ohtahara syndrome
Beschrijving

Neonatal Period Ohtahara syndrome

Datatype

integer

Alias
UMLS CUI [1]
C0393706
Epilepsy of infancy with migrating focal seizures
Beschrijving

Epilepsy of infancy with migrating focal seizures

Datatype

integer

Alias
UMLS CUI [1,1]
C1858477
UMLS CUI [1,2]
C0231330
West syndromes
Beschrijving

Infancy West syndrome

Datatype

integer

Alias
UMLS CUI [1]
C0037769
Myoclonic epilepsy in infancy (MEI)
Beschrijving

Infancy MEI

Datatype

integer

Alias
UMLS CUI [1]
C0917800
Benign infantile epilepsy
Beschrijving

Benign infantile epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0751120
Benign familial infantile epilepsy
Beschrijving

Benign familial infantile epilepsy

Datatype

integer

Alias
UMLS CUI [1,1]
C0391958
UMLS CUI [1,2]
C0205183
UMLS CUI [1,3]
C0231330
Dravet syndrome
Beschrijving

Infancy Dravet syndrome

Datatype

integer

Alias
UMLS CUI [1]
C0751122
Myoclonic encephalopathy in nonprogressive disorders
Beschrijving

Infancy Myoclonic encephalopathy in nonprogressive disorders

Datatype

integer

Alias
UMLS CUI [1]
C0270855
Childhood Febrile seizures plus
Beschrijving

Childhood Febrile seizures plus

Datatype

integer

Alias
UMLS CUI [1]
C0009952
Early onset benign childhood occipital epilepsy (Panayiotopoulos type)
Beschrijving

Benign childhood occipital epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0393676
Childhood Epilepsy with myoclonic atonic seizures
Beschrijving

Epilepsy with myoclonic atonic seizures

Datatype

integer

Alias
UMLS CUI [1]
C0393702
Benign childhood epilepsy with centrotemporal spikes (BCECTS)
Beschrijving

Benign childhood epilepsy BCECTS

Datatype

integer

Alias
UMLS CUI [1]
C2363129
Autosomal-dominant nocturnal frontal lobe epilepsy (ADNFLE)
Beschrijving

Nocturnal frontal lobe epilepsy ADNFLE

Datatype

integer

Alias
UMLS CUI [1]
C3696898
Late onset childhood occipital epilepsy (Gastaut type)
Beschrijving

Late onset childhood occipital epilepsy (Gastaut type)

Datatype

integer

Alias
UMLS CUI [1]
C0393677
Epilepsy with myoclonic absences
Beschrijving

Childhood Epilepsy with myoclonic absences

Datatype

integer

Alias
UMLS CUI [1]
C0393703
Lennox-Gastaut syndrome
Beschrijving

Lennox-Gastaut syndrome

Datatype

integer

Alias
UMLS CUI [1]
C0238111
Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)
Beschrijving

Epileptic encephalopathy CSWS

Datatype

integer

Alias
UMLS CUI [1]
C3806403
Landau-Kleffner syndrome (LKS)
Beschrijving

Landau-Kleffner syndrome (LKS)

Datatype

integer

Alias
UMLS CUI [1]
C0282512
Childhood absence epilepsy (CAE)
Beschrijving

Childhood absence epilepsy (CAE)

Datatype

integer

Alias
UMLS CUI [1]
C3263988
Juvenile absence epilepsy (JAE)
Beschrijving

Adolescence – Adult JAE

Datatype

integer

Alias
UMLS CUI [1]
C1833495
Other familial temporal lobe epilepsies
Beschrijving

Other familial temporal lobe epilepsies

Datatype

integer

Alias
UMLS CUI [1]
C1842564
Juvenile myoclonic epilepsy
Beschrijving

Juvenile myoclonic epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0270853
Progressive myoclonus epilepsies
Beschrijving

Progressive myoclonus epilepsies

Datatype

integer

Alias
UMLS CUI [1]
C0751778
Autosomal Dominant Epilepsy with Auditory Features (ADEAF)
Beschrijving

Autosomal Dominant Epilepsy with Auditory Features (ADEAF)

Datatype

integer

Alias
UMLS CUI [1]
C1838062
Epilepsy with generalized tonic-clonic seizures alone
Beschrijving

Epilepsy with generalized tonic-clonic seizures alone

Datatype

integer

Alias
UMLS CUI [1]
C1843234
Familial focal epilepsy with variable foci (childhood to adult)
Beschrijving

Familial focal epilepsy with variable foci (childhood to adult)

Datatype

integer

Alias
UMLS CUI [1]
C1858477
Reflex epilepsies
Beschrijving

Reflex epilepsies

Datatype

integer

Alias
UMLS CUI [1]
C0270857
Mesial temporal lobe epilepsy
Beschrijving

Mesial temporal lobe epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C1968848
Rasmussen syndrome
Beschrijving

Rasmussen syndrome

Datatype

integer

Alias
UMLS CUI [1]
C0393484
Gelastic seizures with hypothalamic hamartoma
Beschrijving

Gelastic seizures with hypothalamic hamartoma

Datatype

integer

Alias
UMLS CUI [1,1]
C0270820
UMLS CUI [1,2]
C0342418
Temporal lobe epilepsy
Beschrijving

Temporal lobe epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0014556
Frontal lobe epilepsy
Beschrijving

Frontal lobe epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0085541
Occipital lobe epilepsy
Beschrijving

Occipital lobe epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0393691
Parietal lobe epilepsy
Beschrijving

Parietal lobe epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0393690
Focal epilepsy (specific localization unknown)
Beschrijving

Focal epilepsy (specific localization unknown)

Datatype

integer

Alias
UMLS CUI [1]
C0014547
The epilepsy does not fit into one of these specific electro-clinical or distinctive constellations categories
Beschrijving

Unspecified epilepsy

Datatype

integer

Alias
UMLS CUI [1]
C0154722
If two or more epilepsy syndromes were selected as present, rate the confidence level that these are distinct syndromes
Beschrijving

Confidence level

Datatype

integer

Alias
UMLS CUI [1]
C0518578

Similar models

Classification of Etiology,Seizures and syndromes by age of onset

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Classification of Etiology
Item
Genetic or presumed genetic OR epilepsy of unknown cause
integer
C2724370 (UMLS CUI [1])
Code List
Genetic or presumed genetic OR epilepsy of unknown cause
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Structural or metabolic
integer
C2724370 (UMLS CUI [1])
Code List
Structural or metabolic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item Group
Specific Etiology
Item
Viral, bacterial and parasitic infections
integer
C0009450 (UMLS CUI [1])
Code List
Viral, bacterial and parasitic infections
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Viral, bacterial and parasitic infections
integer
C0009450 (UMLS CUI [1])
Code List
Viral, bacterial and parasitic infections
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Infections
Item
Viral, bacterial and parasitic infections: If more than one specific etiology, please specify
text
C0009450 (UMLS CUI [1])
Item
Traumatic brain injury
integer
C0876926 (UMLS CUI [1])
Code List
Traumatic brain injury
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Traumatic brain injury
integer
C0876926 (UMLS CUI [1])
Code List
Traumatic brain injury
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Traumatic brain injury
Item
Traumatic brain injury: If more than one specific etiology is selected, specify
text
C0876926 (UMLS CUI [1])
Item
Stroke
integer
C0038454 (UMLS CUI [1])
Code List
Stroke
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Stroke
integer
C0038454 (UMLS CUI [1])
Code List
Stroke
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Stroke
Item
Stroke: If more than one specific etiology is selected, specify:
text
C0038454 (UMLS CUI [1])
Item
Intraventricular hemorrhage
integer
C0240059 (UMLS CUI [1])
Code List
Intraventricular hemorrhage
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Intraventricular hemorrhage
integer
C0240059 (UMLS CUI [1])
Code List
Intraventricular hemorrhage
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Intraventricular hemorrhage
Item
Intraventricular hemorrhage: If more than one specific etiology is selected, specify:
text
C0240059 (UMLS CUI [1])
Item
Hypoxic-ischemic encephalopathy
integer
C0149878 (UMLS CUI [1])
Code List
Hypoxic-ischemic encephalopathy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Hypoxic-ischemic encephalopathy
integer
C0149878 (UMLS CUI [1])
Code List
Hypoxic-ischemic encephalopathy
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Hypoxic-ischemic encephalopathy
Item
Hypoxic-ischemic encephalopathy: If more than one specific etiology is selected, specify:
text
C0149878 (UMLS CUI [1])
Item
Other metabolic or toxic insults
integer
C0600688 (UMLS CUI [1])
C0006112 (UMLS CUI [2])
Code List
Other metabolic or toxic insults
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Other metabolic or toxic insults
integer
C0600688 (UMLS CUI [1])
C0006112 (UMLS CUI [2])
Code List
Other metabolic or toxic insults
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Other metabolic or toxic insults
Item
Other metabolic or toxic insults:If more than one specific etiology is selected, specify:
text
C0600688 (UMLS CUI [1])
C0006112 (UMLS CUI [2])
Item
Neurocutaneous syndromes
integer
C0265316 (UMLS CUI [1])
Code List
Neurocutaneous syndromes
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Neurocutaneous syndromes
integer
C0265316 (UMLS CUI [1])
Code List
Neurocutaneous syndromes
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Neurocutaneous syndromes
Item
Neurocutaneous syndromes: If more than one specific etiology is selected, specify:
text
C0265316 (UMLS CUI [1])
Item
Inborn errors of metabolism
integer
C0025521 (UMLS CUI [1])
Code List
Inborn errors of metabolism
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Inborn errors of metabolism
integer
C0025521 (UMLS CUI [1])
Code List
Inborn errors of metabolism
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Inborn errors of metabolism
Item
Inborn errors of metabolism:If more than one specific etiology is selected, specify:
text
C0025521 (UMLS CUI [1])
Item
Genetic and chromosomal development encephalopathies
integer
C0085584 (UMLS CUI [1,1])
C0008626 (UMLS CUI [1,2])
C0314603 (UMLS CUI [1,3])
Code List
Genetic and chromosomal development encephalopathies
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Genetic and chromosomal development encephalopathies
integer
C0085584 (UMLS CUI [1,1])
C0008626 (UMLS CUI [1,2])
C0314603 (UMLS CUI [1,3])
Code List
Genetic and chromosomal development encephalopathies
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Genetic and chromosomal development encephalopathies
Item
Genetic and chromosomal development encephalopathies: If more than one specific etiology is selected, specify
text
C0085584 (UMLS CUI [1,1])
C0008626 (UMLS CUI [1,2])
C0314603 (UMLS CUI [1,3])
Item
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy
integer
C0085584 (UMLS CUI [1,1])
C0458003 (UMLS CUI [1,2])
C1385132 (UMLS CUI [1,3])
Code List
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy
integer
C0085584 (UMLS CUI [1,1])
C0458003 (UMLS CUI [1,2])
C1385132 (UMLS CUI [1,3])
Code List
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Developmental encephalopathy of unknown cause
Item
Developmental encephalopathy of unknown cause as evidenced by the presence of mental retardation, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy: If more than one specific etiology is selected, specify
text
C0085584 (UMLS CUI [1,1])
C0458003 (UMLS CUI [1,2])
C1385132 (UMLS CUI [1,3])
Item
Malformations of cortical or other brain development with or without known genetic determinants
integer
C1955869 (UMLS CUI [1])
C0266449 (UMLS CUI [2])
Code List
Malformations of cortical or other brain development with or without known genetic determinants
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Malformations of cortical or other brain development with or without known genetic determinants
integer
C1955869 (UMLS CUI [1])
C0266449 (UMLS CUI [2])
Code List
Malformations of cortical or other brain development with or without known genetic determinants
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Malformations of cortical or other brain development
Item
Malformations of cortical or other brain development with or without known genetic determinants: If more than one specific etiology is selected, specify
text
C1955869 (UMLS CUI [1])
C0266449 (UMLS CUI [2])
Item
Neoplasia
integer
C1882062 (UMLS CUI [1])
Code List
Neoplasia
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Neoplasia
integer
C1882062 (UMLS CUI [1])
Code List
Neoplasia
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Neoplasia
Item
Neoplasia: If more than one specific etiology is selected, specify
text
C1882062 (UMLS CUI [1])
Item
Mesial temporal sclerosis
integer
C2062593 (UMLS CUI [1])
Code List
Mesial temporal sclerosis
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Mesial temporal sclerosis
integer
C2062593 (UMLS CUI [1])
Code List
Mesial temporal sclerosis
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Mesial temporal sclerosis
Item
Mesial temporal sclerosis: If more than one specific etiology is selected, specify
text
C2062593 (UMLS CUI [1])
Item
Dementia
integer
C0497327 (UMLS CUI [1])
Code List
Dementia
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Dementia
integer
C0497327 (UMLS CUI [1])
Code List
Dementia
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Dementia
Item
Dementia: If more than one specific etiology is selected, specify
text
C0497327 (UMLS CUI [1])
Item
Other degenerative neurologic diseases
integer
C0524851 (UMLS CUI [1])
Code List
Other degenerative neurologic diseases
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Other degenerative neurologic diseases
integer
C0524851 (UMLS CUI [1])
Code List
Other degenerative neurologic diseases
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Genetic or presumed genetic
Item
Genetic or presumed genetic, if known specify:
text
C0017399 (UMLS CUI [1])
Item
Genetic or presumed genetic
integer
C0017399 (UMLS CUI [1])
Code List
Genetic or presumed genetic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Genetic or presumed genetic
integer
C0017399 (UMLS CUI [1])
Code List
Genetic or presumed genetic
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Genetic or presumed genetic,
Item
Genetic or presumed genetic, if more than one specific etiology is selected, specify:
text
C0017399 (UMLS CUI [1])
Item
Epilepsy of unknown cause, without relevant abnormalities on examination, cognition, history, or imaging
integer
C0086237 (UMLS CUI [1])
Code List
Epilepsy of unknown cause, without relevant abnormalities on examination, cognition, history, or imaging
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Epilepsy of unknown cause, without relevant abnormalities on examination, cognition, history, or imaging
integer
C0086237 (UMLS CUI [1])
Code List
Epilepsy of unknown cause, without relevant abnormalities on examination, cognition, history, or imaging
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Epilepsy of unknown cause
Item
Epilepsy of unknown cause without relevant abnormalities on examination, cognition, history, or imaging:If more than one specific etiology is selected, specify
text
C0086237 (UMLS CUI [1])
Other Etiology
Item
Other Etiology, specify:
text
C0205394 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
Item
Other etiology
integer
C0205394 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
Code List
Other etiology
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Other etiology
integer
C0205394 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
Code List
Other etiology
CL Item
Primary cause (1)
CL Item
Secondary cause (2)
Other etiology
Item
Other etiology,If more than one specific etiology is selected, specify:
text
C0205394 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
Item Group
Classification of Seizures
Generalized seizures
Item
Generalized seizures
boolean
C0234533 (UMLS CUI [1])
Item
Tonic clonic seizures (in any combination)
integer
C0748577 (UMLS CUI [1])
Code List
Tonic clonic seizures (in any combination)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Absence
integer
C0014553 (UMLS CUI [1])
Code List
Absence
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Typical
integer
C0311334 (UMLS CUI [1])
Code List
Generalized Seizure Typical
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Atypical
integer
C0595948 (UMLS CUI [1])
Code List
Generalized Seizure Atypical
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Myoclonic absence
integer
C0393703 (UMLS CUI [1])
Code List
Generalized Seizure Myoclonic absence
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Eyelid myoclonia
integer
C4023513 (UMLS CUI [1])
Code List
Generalized Seizure Eyelid myoclonia
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Myoclonic
integer
C0014550 (UMLS CUI [1])
Code List
Generalized Seizure Myoclonic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Myoclonic atonic
integer
C0393702 (UMLS CUI [1])
Code List
Generalized Seizure Myoclonic atonic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Myoclonic tonic
integer
C0014550 (UMLS CUI [1,1])
C0270844 (UMLS CUI [1,2])
Code List
Generalized Seizure Myoclonic tonic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized Seizure Clonic
integer
C0234535 (UMLS CUI [1])
Code List
Generalized Seizure Clonic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized seizures tonic
integer
C0270844 (UMLS CUI [1])
Code List
Generalized seizures tonic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Generalized seizures atonic
integer
C2228222 (UMLS CUI [1])
Code List
Generalized seizures atonic
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Focal seizures
Item
Focal seizures
boolean
C0751495 (UMLS CUI [1])
Item
Focal Seizure without impairment of consciousness or responsiveness
integer
C0751495 (UMLS CUI [1])
Code List
Focal Seizure without impairment of consciousness or responsiveness
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Focal Seizure with observable motor or autonomic components (roughly corresponds to the concept of “simple partial seizure”)
integer
C0016399 (UMLS CUI [1])
Code List
Focal Seizure with observable motor or autonomic components (roughly corresponds to the concept of “simple partial seizure”)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Focal Seizure involving subjective sensory or psychic phenomena only (corresponds to the concept of “aura”)
integer
C0752322 (UMLS CUI [1])
Code List
Focal Seizure involving subjective sensory or psychic phenomena only (corresponds to the concept of “aura”)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Focal Seizure with impairment of consciousness or responsiveness (roughly corresponds to the concept of “complex partial seizure”)
integer
C0270834 (UMLS CUI [1])
Code List
Focal Seizure with impairment of consciousness or responsiveness (roughly corresponds to the concept of “complex partial seizure”)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Focal Seizure evolving to a bilateral, convulsive seizure (involving tonic, clonic, or tonic and clonic components; replaces the term “secondarily generalized seizure”)
integer
C2875090 (UMLS CUI [1])
Code List
Focal Seizure evolving to a bilateral, convulsive seizure (involving tonic, clonic, or tonic and clonic components; replaces the term “secondarily generalized seizure”)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Unclassified Seizure
Item
Unclassified Seizure
boolean
C0270826 (UMLS CUI [1])
Item
Unclassified Seizure Epileptic spasms – focal or generalized
integer
C0270826 (UMLS CUI [1])
Code List
Unclassified Seizure Epileptic spasms – focal or generalized
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Unclassified Seizure
integer
C0270826 (UMLS CUI [1])
Code List
Unclassified Seizure
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
If two or more seizure types were selected as present, rate the confidence level that these are distinct seizure types
integer
C0518578 (UMLS CUI [1])
Code List
If two or more seizure types were selected as present, rate the confidence level that these are distinct seizure types
CL Item
0 No Confidence (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Date of completion
Item
Date of completion of this form
date
C0011008 (UMLS CUI [1])
Information complete
Item
Information complete up to (mm/dd/yyyy)
date
C0205197 (UMLS CUI [1,1])
C0012972 (UMLS CUI [1,2])
Item Group
Syndromes by Age of Onset
Item
Benign familial neonatal epilepsy (BFNE)
integer
C0220669 (UMLS CUI [1])
Code List
Benign familial neonatal epilepsy (BFNE)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Early myoclonic encephalopathy (EME)
integer
C0270855 (UMLS CUI [1])
Code List
Early myoclonic encephalopathy (EME)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Ohtahara syndrome
integer
C0393706 (UMLS CUI [1])
Code List
Ohtahara syndrome
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Epilepsy of infancy with migrating focal seizures
integer
C1858477 (UMLS CUI [1,1])
C0231330 (UMLS CUI [1,2])
Code List
Epilepsy of infancy with migrating focal seizures
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
West syndromes
integer
C0037769 (UMLS CUI [1])
Code List
West syndromes
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Myoclonic epilepsy in infancy (MEI)
integer
C0917800 (UMLS CUI [1])
Code List
Myoclonic epilepsy in infancy (MEI)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Benign infantile epilepsy
integer
C0751120 (UMLS CUI [1])
Code List
Benign infantile epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Benign familial infantile epilepsy
integer
C0391958 (UMLS CUI [1,1])
C0205183 (UMLS CUI [1,2])
C0231330 (UMLS CUI [1,3])
Code List
Benign familial infantile epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Dravet syndrome
integer
C0751122 (UMLS CUI [1])
Code List
Dravet syndrome
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Myoclonic encephalopathy in nonprogressive disorders
integer
C0270855 (UMLS CUI [1])
Code List
Myoclonic encephalopathy in nonprogressive disorders
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Childhood Febrile seizures plus
integer
C0009952 (UMLS CUI [1])
Code List
Childhood Febrile seizures plus
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Early onset benign childhood occipital epilepsy (Panayiotopoulos type)
integer
C0393676 (UMLS CUI [1])
Code List
Early onset benign childhood occipital epilepsy (Panayiotopoulos type)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Childhood Epilepsy with myoclonic atonic seizures
integer
C0393702 (UMLS CUI [1])
Code List
Childhood Epilepsy with myoclonic atonic seizures
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Benign childhood epilepsy with centrotemporal spikes (BCECTS)
integer
C2363129 (UMLS CUI [1])
Code List
Benign childhood epilepsy with centrotemporal spikes (BCECTS)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Autosomal-dominant nocturnal frontal lobe epilepsy (ADNFLE)
integer
C3696898 (UMLS CUI [1])
Code List
Autosomal-dominant nocturnal frontal lobe epilepsy (ADNFLE)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Late onset childhood occipital epilepsy (Gastaut type)
integer
C0393677 (UMLS CUI [1])
Code List
Late onset childhood occipital epilepsy (Gastaut type)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Epilepsy with myoclonic absences
integer
C0393703 (UMLS CUI [1])
Code List
Epilepsy with myoclonic absences
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Lennox-Gastaut syndrome
integer
C0238111 (UMLS CUI [1])
Code List
Lennox-Gastaut syndrome
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)
integer
C3806403 (UMLS CUI [1])
Code List
Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Landau-Kleffner syndrome (LKS)
integer
C0282512 (UMLS CUI [1])
Code List
Landau-Kleffner syndrome (LKS)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Childhood absence epilepsy (CAE)
integer
C3263988 (UMLS CUI [1])
Code List
Childhood absence epilepsy (CAE)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Juvenile absence epilepsy (JAE)
integer
C1833495 (UMLS CUI [1])
Code List
Juvenile absence epilepsy (JAE)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Other familial temporal lobe epilepsies
integer
C1842564 (UMLS CUI [1])
Code List
Other familial temporal lobe epilepsies
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Juvenile myoclonic epilepsy
integer
C0270853 (UMLS CUI [1])
Code List
Juvenile myoclonic epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Progressive myoclonus epilepsies
integer
C0751778 (UMLS CUI [1])
Code List
Progressive myoclonus epilepsies
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Autosomal Dominant Epilepsy with Auditory Features (ADEAF)
integer
C1838062 (UMLS CUI [1])
Code List
Autosomal Dominant Epilepsy with Auditory Features (ADEAF)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Epilepsy with generalized tonic-clonic seizures alone
integer
C1843234 (UMLS CUI [1])
Code List
Epilepsy with generalized tonic-clonic seizures alone
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Familial focal epilepsy with variable foci (childhood to adult)
integer
C1858477 (UMLS CUI [1])
Code List
Familial focal epilepsy with variable foci (childhood to adult)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Reflex epilepsies
integer
C0270857 (UMLS CUI [1])
Code List
Reflex epilepsies
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Mesial temporal lobe epilepsy
integer
C1968848 (UMLS CUI [1])
Code List
Mesial temporal lobe epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Rasmussen syndrome
integer
C0393484 (UMLS CUI [1])
Code List
Rasmussen syndrome
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Gelastic seizures with hypothalamic hamartoma
integer
C0270820 (UMLS CUI [1,1])
C0342418 (UMLS CUI [1,2])
Code List
Gelastic seizures with hypothalamic hamartoma
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Temporal lobe epilepsy
integer
C0014556 (UMLS CUI [1])
Code List
Temporal lobe epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Frontal lobe epilepsy
integer
C0085541 (UMLS CUI [1])
Code List
Frontal lobe epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Occipital lobe epilepsy
integer
C0393691 (UMLS CUI [1])
Code List
Occipital lobe epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Parietal lobe epilepsy
integer
C0393690 (UMLS CUI [1])
Code List
Parietal lobe epilepsy
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
Focal epilepsy (specific localization unknown)
integer
C0014547 (UMLS CUI [1])
Code List
Focal epilepsy (specific localization unknown)
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
The epilepsy does not fit into one of these specific electro-clinical or distinctive constellations categories
integer
C0154722 (UMLS CUI [1])
Code List
The epilepsy does not fit into one of these specific electro-clinical or distinctive constellations categories
CL Item
No (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)
Item
If two or more epilepsy syndromes were selected as present, rate the confidence level that these are distinct syndromes
integer
C0518578 (UMLS CUI [1])
Code List
If two or more epilepsy syndromes were selected as present, rate the confidence level that these are distinct syndromes
CL Item
0 No Confidence (1)
CL Item
Possible (2)
CL Item
Probable (3)
CL Item
Definite (4)
CL Item
Unknown (5)
CL Item
N/A (6)

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