ORPHA:166299

Benign partial epilepsy of infancy with complex partial seizures

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 of infancy with complex partial seizures
fr	Epilepsie bénigne partielle de l'enfant avec crises partielles complexes
de	Benigne Partialepilepsie im Kleinkindalter mit komplexen fokalen Anfällen
es	Epilepsia parcial benigna del lactante con crisis parciales complejas
it	Epilessia parziale benigna dell'infanzia con crisi parziali complesse
nl	Goedaardige partiële epilepsie met complexe partiële insulten op zuigelingenleeftijd
pt	Epilepsia parcial benigna da infância com convulsões parciais complexas
pl	Łagodna niemowlęca padaczka częściowa z napadami złożonymi
cs	Benigní parciální epilepsie dětského věku s komplexními parciálními záchvaty
uk	Доброякісна фокальна епілепсія раннього дитячого віку зі складними фокальними судомами
zh	婴儿良性部分性癫痫伴复杂部分性发作
tr	Kompleks kısmi nöbetler ile seyreden selim kısmi süt çocuğu epilepsisi

Definition in:

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	0015638	E		validated
UMLS	C4749347	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.