familial partial epilepsy
MONDO:0017704Mondo
Findings
No curated finding names familial partial epilepsy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0017704), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- PIK3C2BHGNC:8972
- Moderate · PanelApp Australia · Autosomal dominant · 2025
Where it sits
- Narrower terms (7)
- autosomal dominant epilepsy with auditory features
- familial focal epilepsy with variable foci
- familial sleep-related hypermotor epilepsy
- generalized epilepsy-paroxysmal dyskinesia syndrome
- mesial temporal lobe epilepsy with hippocampal sclerosis
- self-limited epilepsy with centrotemporal spikes
- temporal lobe epilepsy
Other names
2 names
Resolves to: familial partial epilepsy
- Also called
- familial focal epilepsyhereditary partial epilepsy