epilepsy, idiopathic generalized, susceptibility to, 10
Findings
No curated finding names epilepsy, idiopathic generalized, susceptibility to, 10 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 GABRD gene.
Definition from the Mondo Disease Ontology (MONDO:0013103), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
1 feature
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 seizure (within the age range of 3 months to 6 years)HPOHP:0002373
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.
- GABRDHGNC:4084
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · Ambry Genetics · Autosomal dominant · 2018
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
6 names
Resolves to: epilepsy, idiopathic generalized, susceptibility to, 10
- Also called
- EIG10epilepsy, idiopathic generalized, 10epilepsy, idiopathic generalized, susceptibility to, type 10epilepsy, juvenile myoclonic, susceptibility tosusceptibility to idiopathic generalised epilepsy 10susceptibility to idiopathic generalized epilepsy 10