MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
expandepilepsy syndrome (MONDO:0015650)
..Starting node
..expandchildhood-onset epilepsy syndrome ()

       Child Nodes:
........expandacute encephalopathy with inflammation-mediated status epilepticus ()
........expandatypical childhood epilepsy with centrotemporal spikes ()
........expandbenign occipital epilepsy ()
........expandchildhood absence epilepsy ()
........expandcryptogenic late-onset epileptic spasms ()
........expandearly-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation ()
........expandepilepsy with myoclonic absences ()
........expandfamilial partial epilepsy ()
........expandJeavons syndrome ()
........expandLandau-Kleffner syndrome ()
........expandLennox-Gastaut syndrome ()
........expandmyoclonic-astastic epilepsy ()
........expandperioral myoclonia with absences ()
........expandphotosensitive occipital lobe epilepsy ()
........expandprogressive myoclonic epilepsy ()
........expandrolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome ()
........expandrolandic epilepsy-speech dyspraxia syndrome ()



 Sister 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 ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:20072
Name:childhood-onset epilepsy syndrome
Definition:A epilepsy syndrome that occurs during childhood.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:childhood epilepsy syndrome; epilepsy syndrome of childhood; pediatric epilepsy syndrome; pediatric epilepsy syndrome
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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