familial temporal lobe epilepsy 2
MONDO:0011965Mondo
Findings
No curated finding names familial temporal lobe epilepsy 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex or partial seizures and childhood febrile seizures that has material basis in variation in the chromosome region 12q22-q23.3.
Definition from the Mondo Disease Ontology (MONDO:0011965), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
2 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.
- Febrile status epilepticusHPOHP:0032656
- 4 of 7 reported patients
- Bilateral tonic-clonic seizureHPOHP:0002069
Where it sits
- A kind of
Other names
2 names
Resolves to: familial temporal lobe epilepsy 2
- Also called
- ETL2familial temporal lobe epilepsy type 2