MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
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Parent Node:
expandbrain disease (MONDO:0005560)
..Starting node
..expandepilepsy ()

       Child Nodes:
........expandarthrogryposis epileptic seizures migrational brain disorder ()
........expandcerebral diseases of vascular origin with epilepsy ()
........expandcerebral malformation with epilepsy ()
........expandchromosomal anomaly with epilepsy as a major feature ()
........expandCoffin-Lowry syndrome ()
........expandelectroclinical syndrome ()
........expandepilepsia partialis continua ()
........expandepilepsy syndrome ()
........expandextratemporal epilepsy ()
........expandgeneralised epilepsy ()
........expandidiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes ()
........expandimmune epilepsy ()
........expandinfectious disease with epilepsy ()
........expandinflammatory and autoimmune disease with epilepsy ()
........expandmetabolic disease with epilepsy ()
........expandmetabolic epilepsy ()
........expandmonogenic disease with epilepsy ()
........expandpartial epilepsy ()
........expandpost-traumatic epilepsy ()
........expandstatus epilepticus ()
........expandstructural epilepsy ()
........expandvariable age onset epilepsy ()



 Sister Nodes: 
..expandakinetic mutism ()
..expandautoimmune encephalopathy with parasomnia and obstructive sleep apnea ()
..expandbasal ganglia disease ()
..expandbrain compression ()
..expandbrain edema ()
..expandbrain hypoxia - ischemia ()
..expandbrain inflammatory disease ()
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..expandbrain neoplasm ()
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..expandcerebral sarcoidosis ()
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..expandCOL4A1-related familial vascular leukoencephalopathy ()
..expandcolpocephaly ()
..expandcorpus callosum agenesis of blepharophimosis robin type ()
..expandcorpus callosum dysgenesis cleft spasm ()
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..expanddelayed encephalopathy after acute carbon monoxide poisoning ()
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..expanddisorder of optic chiasm ()
..expandencephalomalacia ()
..expandencephalopathy due to defective mitochondrial and peroxisomal fission ()
..expandencephalopathy, acute, infection-induced ()
..expandencephalopathy, recurrent, of childhood ()
..expandepilepsy ()
..expandhepatic encephalopathy ()
..expandhydrocephalus ()
..expandintracranial hypertension ()
..expandintracranial hypotension ()
..expandkernicterus ()
..expandleukoencephalopathy, megalencephalic ()
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..expandnarcolepsy without cataplexy ()
..expandnarcolepsy-cataplexy syndrome ()
..expandneurometabolic disease ()
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..expandprion disease ()
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..expandsubarachnoid hemorrhage (disease) ()
..expandthalamic disease ()
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..expandvisual pathway disease ()
..expandWernicke encephalopathy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:5027
Name:epilepsy
Definition:A brain disorder characterized by episodes of abnormally increased neuronal discharge resulting in transient episodes of sensory or motor neurological dysfunction, or psychic dysfunction. These episodes may or may not be associated with loss of consciousness or convulsions.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:epilepsy syndrome; epileptic syndrome; seizure disorder
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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