MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandepilepsy (MONDO:0005027)
..Starting node
..expandepilepsy syndrome ()

       Child Nodes:
........expandadolescent-onset epilepsy syndrome ()
........expandadolescent/adult-onset epilepsy syndrome ()
........expandatherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome ()
........expandchildhood-onset epilepsy syndrome ()
........expandcortical dysplasia-focal epilepsy syndrome ()
........expandDEND syndrome ()
........expandepilepsy-telangiectasia syndrome ()
........expandepileptic encephalopathy, infantile or early childhood ()
........expandinfantile epilepsy syndrome ()
........expandMoynahan syndrome ()
........expandneonatal epilepsy syndrome ()
........expandneonatal/infantile epilepsy syndrome ()
........expandoculocerebrocutaneous syndrome ()
........expandPallister-W syndrome ()
........expandPEHO syndrome ()



 Sister 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 ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15650
Name:epilepsy syndrome
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:syndromic epilepsy
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal