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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|---|
| 248 | ALPI | alkaline phosphatase, intestinal | |
| 250 | ALPP | alkaline phosphatase, placental | |
| 821 | CANX | calnexin | |
| 2923 | PDIA3 | protein disulfide isomerase family A member 3 | |
| 4886 | NPY1R | neuropeptide Y receptor Y1 | |
| 5332 | PLCB4 | phospholipase C beta 4 | |
| 6513 | SLC2A1 | solute carrier family 2 member 1 | |
| 9254 | CACNA2D2 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | |
| 84720 | PIGO | phosphatidylinositol glycan anchor biosynthesis class O |
Related Glycoprotein
