raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98260

OBSOLETE: Adolescent-onset epilepsy syndrome

inactive · referred to ORPHA:166463Epilepsy 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 Epilepsy syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Adolescent-onset epilepsy syndrome
frOBSOLETE : Syndrome épileptique de l'adolescence
deOBSOLET: Epilepsie-Syndrom, im Erwachsenenalter beginnend
esOBSOLETO: Síndrome de epilepsia de inicio en la adolescencia
itOBSOLETO: Sindrome epilettica con esordio nell'adolescenza
nlOBSOLEET: Epilepsiesyndroom met aanvang in de adolescentie
ptOBSOLETO: Síndrome epilepsia de início na adolescência
plNIEAKTUALNE: Zespół padaczkowy okresu młodzieńczego
csNEAKTUÁLNÍ: Epileptické syndromy s nástupem v dospívání
ukСиндром підліткової епілепсії
zh成人迟发型癫痫综合征
trAdolesan başlangıçlı 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