Epilepsy etiology primary type

General Details:

Name:
Epilepsy etiology primary type
Steward:
NINDS
Definition:
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).
Registration Status:
Qualified

Permissible Values:

Data Type:
Value List
Unit of Measure:
Ids:
Value Code Name Code Code System Code Description
Idiopathic generalized with known syndrome Idiopathic generalized with known syndrome Idiopathic generalized with known syndrome (childhood and juvenile absence epilepsy, juvenile myoclonic epilepsy, generalized GTCS alone)
Other generalized epilepsy known or presumed to be genetic but not meeting criteria for an idiopathic generalized epilepsy syndrome Other generalized epilepsy known or presumed to be genetic but not meeting criteria for an idiopathic generalized epilepsy syndrome Other generalized epilepsy known or presumed to be genetic but not meeting criteria for an idiopathic generalized epilepsy syndrome (e.g., Doose Syndrome)
Known genetic mutation with or without developmental /epileptic encephalopathy or known disease/syndrome linked to genetic mutation Known genetic mutation with or without developmental /epileptic encephalopathy or known disease/syndrome linked to genetic mutation Known genetic mutation with or without developmental /epileptic encephalopathy (e.g., CDKL5) or known disease/syndrome linked to genetic mutation (e.g., Dravet syndrome)
Focal epilepsy with or without a known proven mutation Focal epilepsy with or without a known proven mutation Focal epilepsy with or without a known proven mutation (e.g., LGI1, ADNFL)
Genetic epilepsies not otherwise specified Genetic epilepsies not otherwise specified Genetic epilepsies not otherwise specified
Traumatic brain injury Traumatic brain injury Traumatic brain injury
Stroke Stroke Stroke
Intraventricular hemorrhage Intraventricular hemorrhage Intraventricular hemorrhage
Hypoxic-ischemic encephalopathy Hypoxic-ischemic encephalopathy Hypoxic-ischemic encephalopathy
Neurocutaneous syndromes Neurocutaneous syndromes Neurocutaneous syndromes (e.g., tuberous sclerosis, neurofibromatosis)
Developmental/epileptic encephalopathy of unknown cause Developmental/epileptic encephalopathy of unknown cause Developmental/epileptic encephalopathy of unknown cause as evidenced by the presence of intellectual disability, cerebral palsy, or autism with no evidence of a specific insult of disorder to which cause can be attributed preceding the onset of epilepsy
Malformations of cortical or other brain development with or without known genetic determinants Malformations of cortical or other brain development with or without known genetic determinants Malformations of cortical or other brain development with or without known genetic determinants
Neoplasia Neoplasia Neoplasia
Mesial Temporal Sclerosis Mesial Temporal Sclerosis Mesial Temporal Sclerosis
Dementia Dementia Dementia
Other degenerative neurologic diseases Other degenerative neurologic diseases Other degenerative neurologic diseases
Structural, other Structural, other Structural, other (e.g., encephalocele, structural abnormality of unknown cause)

Designations:

Designation:
Epilepsy etiology primary type
Tags:

Designations:

Definition:
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).
Tags:

Reference Documents:

ID:
Title:
URI:
Provider Org:
Language Code:
Document:
Berg AT, Berkovic SF, Brodie MJ, Buchhalter J, et al. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009. Epilepsia. 2010 Apr;51(4):676-85. http://www.ilae-epilepsy.org/Visitors/Centre/ctf/ctfoverview.cfm

Identifiers:

Source:
NLM
Id:
3Rys_UvtnWH
Version:
1.1
Source:
NINDS
Id:
C14426
Version:
1
Source:
BRICS Variable Name
Id:
EpilEtioPrimryTyp
Version: