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:
expandinfantile epilepsy syndrome (MONDO:0020071)
Parent Node:
expandneonatal epilepsy syndrome (MONDO:0020070)
..Starting node
..expandundetermined early-onset epileptic encephalopathy ()

       Child Nodes:
........expandepileptic encephalopathy, early infantile, 13 ()
........expandepileptic encephalopathy, early infantile, 21 ()
........expandepileptic encephalopathy, early infantile, 24 ()
........expandepileptic encephalopathy, early infantile, 25 ()
........expandepileptic encephalopathy, early infantile, 26 ()
........expandepileptic encephalopathy, early infantile, 28 ()
........expandepileptic encephalopathy, early infantile, 29 ()
........expandepileptic encephalopathy, early infantile, 31 ()
........expandepileptic encephalopathy, early infantile, 32 ()
........expandepileptic encephalopathy, early infantile, 33 ()
........expandepileptic encephalopathy, early infantile, 41 ()
........expandepileptic encephalopathy, early infantile, 42 ()
........expandepileptic encephalopathy, early infantile, 44 ()
........expandepileptic encephalopathy, early infantile, 45 ()
........expandepileptic encephalopathy, early infantile, 46 ()
........expandepileptic encephalopathy, early infantile, 47 ()



 Sister Nodes: 
..expandbenign idiopathic neonatal seizures ()
..expandbenign neonatal seizures ()
..expandepileptic encephalopathy with global cerebral demyelination ()  LSDB  L: 00107;
..expandmalignant migrating partial seizures of infancy ()
..expandsevere neonatal-onset encephalopathy with microcephaly ()
..expandundetermined early-onset epileptic encephalopathy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18614
Name:undetermined early-onset epileptic encephalopathy
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:undetermined EOEE
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal