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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
brain disease +     
Acute Febrile Encephalopathy 
akinetic mutism 
alveolar echinococcosis  
amblyopia +   
Athabaskan brainstem dysgenesis syndrome  
basal ganglia disease +   
baylisascariasis 
Beta-Ureidopropionase Deficiency  
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
Brain Abscess +   
brain compression  
Brain Death  
brain edema +   
Brain Hypoxia +   
Brain Injuries +   
Brain Neoplasms +   
Central Auditory Diseases +   
central nervous system origin vertigo 
cerebellar disease +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
Chronic Brain Damage +   
Colpocephaly 
complex cortical dysplasia with other brain malformations +   
Congenital Cerebral Granulomas 
Crome Syndrome 
cystic echinococcosis  
dementia +   
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
encephalitis +   
encephalomalacia +   
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM  
epilepsy +   
A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313)
Headache Disorders +   
hepatic encephalopathy +   
heterophyiasis 
hydrocephalus +   
hypoglycemic coma 
hypothalamic disease +   
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly  
intracranial hypertension +   
intracranial hypotension 
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kuzniecky Andermann Syndrome 
Leukoencephalopathies +   
lymphocytic choriomeningitis  
Metabolic Brain Diseases +   
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
movement disease +   
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
neuroschistosomiasis 
Non-Lissencephalic Cortical Dysplasia 
paragonimiasis 
phaeohyphomycosis +  
prion disease +   
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Encephalopathy, with or without Lipodystrophy  
Pseudo-TORCH Syndrome +   
pseudobulbar palsy +   
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
sparganosis 
Spastic Pseudosclerosis 
Subdural Effusion 
tertiary neurosyphilis +  
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
transient global amnesia 
Wernicke encephalopathy  
 focal epilepsy +   
 visual epilepsy +   

Synonyms
Exact Synonyms: Epilepsies ;   Epileptic Seizure ;   Epileptic Seizures ;   Seizures ;   aura ;   auras ;   awakening epilepsy ;   cryptogenic epilepsies ;   cryptogenic epilepsy ;   epilepsy syndrome ;   epileptic syndrome ;   seizure disorder ;   seizure disorders ;   single seizure ;   single seizures
Narrow Synonyms: EPILEPSY, MITOCHONDRIAL ;   Epilepsy, benign familial juvenile ;   INTRACTABLE SEIZURE
Related Synonyms: sudden unexpected death in epilepsy
Primary IDs: MESH:D004827
Alternate IDs: MESH:D000080485 ;   OMIA:001596
Xrefs: ICD10CM:G40.909 ;   ICD9CM:345.9 ;   NCI:C3020 ;   OMIM:PS613339
Definition Sources: http://books.google.com/books?id=YXqX04Te9ioC&printsec=frontcover&source=gbs_ge_summary_r&cad=0#v=onepage&q&f=false "DO", http://www.merriam-webster.com/medlineplus/epilepsy "DO", MESH:D004827

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