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:
expandcentral nervous system infectious disorder (MONDO:0024619)
Parent Node:
expandepilepsy (MONDO:0005027)
..Starting node
..expandinfectious disease with epilepsy ()

       Child Nodes:
........expandacute disseminated encephalomyelitis ()
........expandColorado tick fever ()
........expandcongenital rubella syndrome ()
........expandcongenital toxoplasmosis ()
........expandeastern equine encephalitis ()
........expandencephalitis lethargica ()
........expandfetal cytomegalovirus syndrome ()
........expandJapanese encephalitis ()
........expandKluver-Bucy syndrome ()
........expandla Crosse encephalitis ()
........expandmeningococcal meningitis ()
........expandMycoplasma encephalitis ()
........expandpneumococcal meningitis ()
........expandprogressive rubella panencephalitis ()
........expandst. Louis encephalitis ()
........expandsubacute sclerosing panencephalitis ()
........expandtick-borne encephalitis ()
........expandWest-Nile encephalitis ()
........expandwestern equine encephalitis ()



 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:15659
Name:infectious disease with epilepsy
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal