epilepsy, idiopathic generalized, susceptibility to, 11
MONDO:0011875Mondo
Findings
No curated finding names epilepsy, idiopathic generalized, susceptibility to, 11 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An inherited susceptibility or predisposition to developing epilepsy, idiopathic generalized, in which the cause of the disease is a mutation in the CLCN2 gene.
Definition from the Mondo Disease Ontology (MONDO:0011875), 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.
- CLCN2HGNC:2020
- Strong · Genomics England PanelApp · Autosomal dominant · 2021
Where it sits
Other names
6 names
Resolves to: epilepsy, idiopathic generalized, susceptibility to, 11
- Also called
- CLCN2 generalised epilepsyCLCN2 generalized epilepsyEIG11epilepsy, idiopathic generalized, susceptibility to, type 11generalised epilepsy caused by mutation in CLCN2generalized epilepsy caused by mutation in CLCN2