Benign familial infantile epilepsy

Go to external page http://www.orpha.net/ORDO/Orphanet_306


Benign familial infantile epilepsy (BFIE) is a genetic epileptic syndrome characterized by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life.

Synonyms:

BFIS

Benign familial infantile convulsions

Benign familial infantile seizures

BFIE

This is just here as a test because I lose it

Term information

expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=306
hasDbXref
  • OMIM:601764
  • OMIM:605751
  • OMIM:607745
  • OMIM:617080
  • UMLS:C0220669
  • ICD-10:G40.3
  • OMIM:612627
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_409929
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
notation
  • ORPHA:306
part of
  • http://www.orpha.net/ORDO/Orphanet_98746
  • http://www.orpha.net/ORDO/Orphanet_166311
  • http://www.orpha.net/ORDO/Orphanet_98744
  • http://www.orpha.net/ORDO/Orphanet_166475
present in
  • http://www.orpha.net/ORDO/Orphanet_409991