epilepsy, idiopathic generalized, susceptibility to, 13
MONDO:0012627Mondo
Findings
No curated finding names epilepsy, idiopathic generalized, susceptibility to, 13 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 juvenile myclonic epilepsy, idiopathic generalized epilepsy, or childhood absence epilepsy in which the cause of the disease is a mutation in the GABRA1 gene.
Definition from the Mondo Disease Ontology (MONDO:0012627), 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.
- GABRA1HGNC:4075
- Strong · G2P · Autosomal dominant · 2015
Where it sits
- A kind of
Other names
4 names
Resolves to: epilepsy, idiopathic generalized, susceptibility to, 13
- Also called
- EIG13epilepsy, idiopathic generalized, susceptibility to, type 13susceptibility to idiopathic generalised epilepsy 13susceptibility to idiopathic generalized epilepsy 13