Non-specific early-onset epileptic encephalopathy

Go to external page http://www.orpha.net/ORDO/Orphanet_442835


A rare infantile epilepsy syndrome characterized by early onset of seizures of variable type and severity, potentially associated with a spectrum of clinical signs and symptoms including delay or lack of psychomotor development, intellectual disability, poor or absent speech development, behavioral abnormalities, hypotonia, movement disorders, spasticity, microcephaly, and dysmorphic facial features, among others. Brain imaging findings are also variable and may include cerebral atrophy or white matter abnormalities.

Synonyms:

Undetermined early-onset epileptic encephalopathy

Non-specific EOEE

Undetermined EOEE

This is just here as a test because I lose it

Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=442835
hasDbXref
  • OMIM:616056
  • OMIM:617166
  • OMIM:618559
  • OMIM:616366
  • OMIM:619124
  • OMIM:615833
  • OMIM:618916
  • OMIM:615476
  • ICD-10:G40.4
  • OMIM:617829
  • OMIM:618437
  • OMIM:618396
  • OMIM:617854
  • OMIM:618008
  • OMIM:616339
  • OMIM:618959
  • OMIM:618012
  • OMIM:617153
  • OMIM:614558
  • OMIM:301058
  • OMIM:617836
  • OMIM:616211
  • OMIM:618557
  • OMIM:616409
  • OMIM:617020
  • OMIM:615905
  • OMIM:617830
  • OMIM:301008
  • OMIM:615871
  • OMIM:617938
  • OMIM:618468
  • OMIM:618201
  • OMIM:617106
  • OMIM:617831
  • OMIM:617162
  • OMIM:616346
  • OMIM:618910
  • OMIM:617105
  • OMIM:617132
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409945
  • http://www.orpha.net/ORDO/Orphanet_409944
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409941
  • http://www.orpha.net/ORDO/Orphanet_409929
  • http://www.orpha.net/ORDO/Orphanet_409932
  • http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
notation
  • ORPHA:442835
part of
  • http://www.orpha.net/ORDO/Orphanet_98749
  • http://www.orpha.net/ORDO/Orphanet_98745
  • http://www.orpha.net/ORDO/Orphanet_611314
  • http://www.orpha.net/ORDO/Orphanet_98746
  • http://www.orpha.net/ORDO/Orphanet_98258
  • http://www.orpha.net/ORDO/Orphanet_98744
  • http://www.orpha.net/ORDO/Orphanet_98257
present in
  • http://www.orpha.net/ORDO/Orphanet_409991

Term relations

Subclass of:
Related from:
disease-causing germline mutation(s) in