familial temporal lobe epilepsy 6
MONDO:0014308Mondo
Findings
No curated finding names familial temporal lobe epilepsy 6 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A temporal lobe epilepsy that has material basis in variation in the chromosome region 3q25-q26.
Definition from the Mondo Disease Ontology (MONDO:0014308), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
5 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Focal impaired awareness seizureHPOHP:0002384
- 5 of 11 reported patients
- Bilateral tonic-clonic seizure with focal onsetHPOHP:0007334
- 4 of 11 reported patients
- Febrile seizure (within the age range of 3 months to 6 years)HPOHP:0002373
- 4 of 11 reported patients
- Focal aware seizureHPOHP:0002349
- 4 of 11 reported patients
- Status epilepticusHPOHP:0002133
- 2 of 11 reported patients
Where it sits
Other names
2 names
Resolves to: familial temporal lobe epilepsy 6
- Also called
- ETL6familial temporal lobe epilepsy type 6