raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:165805

Familial mesial temporal lobe epilepsy with febrile seizures

inactive · moved to ORPHA:36387Genetic epilepsy with febrile seizure plus

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Genetic epilepsy with febrile seizure plus

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFamilial mesial temporal lobe epilepsy with febrile seizures
frEpilepsie temporale mésiale familiale avec convulsions fébriles
deTemporallappenepilepsie, mesiale, mit Fieberkrämpfen, familiäre Form
esEpilepsia familiar mesial temporal con crisis febriles
itEpilessia mesiale temporale familiare con convulsioni febbrili
nlFamiliale mesiale temporaalkwabepilepsie met febriele epileptische aanvallen
ptEpilepsia temporal mesial familiar com convulsões febris
plRodzinna padaczka przyśrodkowego płata skroniowego z drgawkami gorączkowymi
csFamiliární meziální epilepsie spánkového laloku s febrilními záchvatyFamiliární epileptický syndrom · Generalizovaná epilepsie s febrilními záchvaty
ukСімейна мезіальна скронева епілепсія з фебрильними нападами
zh家族性近中颞叶癫痫伴发热性惊厥发作
trAteşli nöbetler ile seyreden ailesel mezyal temporal lob epilepsisi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0013742Evalidated
UMLSC5191318Evalidated

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

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