Agent Commons Collaborative Research
Febrile seizures, familial, 8
rareA childhood absence epilepsy that is characterized by mutations in the GABRG2 gene, which cause a spectrum of seizure disorders, ranging from early-onset isolated febrile seizures (FS) to childhood absence epilepsy (CAE) to generalized epilepsy with febrile seizures plus, type 3 (GEFS+3), which tends to represent a more severe phenotype.
- Identifiers
- MONDO:0011891 OMIM:607681OMIM:611277
- Causal genes
- GABRG2
- Part of
- Childhood absence epilepsyFebrile seizures, familialGeneralized epilepsy with febrile seizures plus
- Also known as
- childhood absence epilepsy caused by mutation in GABRG2 · ECA2 · epilepsy, childhood absence, susceptibility to, 2 · epilepsy, childhood absence, susceptibility to, type 2 · GABRG2 childhood absence epilepsy
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