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childhood absence epilepsy
Summary
- Synonym
-
- petit mal seizure
- pyknolepsy
- Definition
- A childhood electroclinical syndrome that is characterized by brief and frequent absence seizures in children with age of onset between four and ten years.
- Super Class
- childhood electroclinical syndrome
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2562 | GABRB3 | gamma-aminobutyric acid type A receptor subunit beta3 | |
| 2566 | GABRG2 | gamma-aminobutyric acid type A receptor subunit gamma2 | |
| 2897 | GRIK1 | glutamate ionotropic receptor kainate type subunit 1 | |
| 6513 | SLC2A1 | solute carrier family 2 member 1 | |
| 8912 | CACNA1H | calcium voltage-gated channel subunit alpha1 H | |
| 163175 | LGI4 | leucine rich repeat LGI family member 4 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P21555 | Neuropeptide Y receptor type 1 | |
| P32305 | 5-hydroxytryptamine receptor 7 | |
| P54282 | Voltage-dependent P/Q-type calcium channel subunit alpha-1A | |
| Q63634 | Neuropeptide Y receptor type 5 |
