raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98258

OBSOLETE: Infantile epilepsy syndrome

inactive · referred to ORPHA:693802Neonatal/infantile-onset epilepsy syndrome

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Neonatal-infantile onset epilepsy syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Infantile epilepsy syndrome
frOBSOLETE : Syndrome épileptique du nourrisson
deOBSOLET: Epilepsie-Syndrom, infantiles
esOBSOLETO: Síndrome epiléptico infantil
itOBSOLETO: Sindrome epilettica infantile
nlOBSOLEET: Infantiele epilepsiesyndroom
ptOBSOLETO: Síndrome epilepsia do lactente
plNIEAKTUALNE: Zespół padaczkowy okresu niemowlęcego
csNEAKTUÁLNÍ: Kojenecké epileptické syndromy
ukСиндром інфантильної епілепсії
zh婴幼儿癫痫综合征
trİnfantil epilepsi sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card