ORPHA:166302

Benign partial epilepsy with secondarily generalized seizures in infancy

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Self-limited infantile epilepsy

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Benign partial epilepsy with secondarily generalized seizures in infancy
fr	Epilepsie partielle bénigne du nourrisson avec crises généralisées secondaires
de	Benigne Partialepilepsie der frühen Kindheit mit sekundär generalisierten Anfällen
es	Epilepsia parcial benigna del lactante con crisis generalizadas secundarias
it	Epilessia parziale benigna dell'infanzia con convulsioni generalizzate secondarie
nl	Goedaardige partiële epilepsie met secundair gegeneraliseerde insulten op zuigelingenleeftijd
pt	Epilepsia parcial benigna da infância com generalização secundária
pl	Łagodna padaczka częściowa z wtórnie uogólnionymi napadami w okresie niemowlęcym
cs	Benigní parciální epilepsie se sekundárně generalizovanými záchvaty v dětství
uk	Доброякісна фокальна епілепсія раннього дитячого віку з вторинно генералізованими судомами
zh	婴儿良性部分性癫痫伴继发全身性发作
tr	Süt çocuğunda sekonder jeneralize nöbetler ile seyreden selim kısmi epilepsi

Definition in:

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	0015639	E		validated
UMLS	C4749728	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

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