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benign familial infantile epilepsy

Go to external page http://purl.obolibrary.org/obo/MONDO_0017615

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. [ Orphanet:306 ]

Synonyms: benign familial infantile convulsions BFIS BFIC benign familial infantile seizures benign familial infantile convulsion benign familial infantile epilepsy BFIE seizures, benign familial infantile

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:V17.2 (MONDO:relatedTo)
  • GARD:857 (Orphanet:306)
  • Orphanet:306 (MONDO:equivalentTo)
  • SCTID:230410004 (MONDO:equivalentTo)
  • DOID:0060169 (MONDO:equivalentTo)
  • OMIMPS:601764 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

exactMatch

http://purl.obolibrary.org/obo/DOID_0060169

http://www.orpha.net/ORDO/Orphanet_306

https://omim.org/phenotypicSeries/PS601764

http://identifiers.org/snomedct/230410004

id

MONDO:0017615

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0017615