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
External Links
Disease Ontology
DOID:1825
MeSH
UMLS
NCI Thesaurus
Related Genes
Displaying all 9 entries
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
Displaying 1 entry
Gene ID Gene Symbol Description Source
18166 Npy1r neuropeptide Y receptor Y1

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Acknowledgements

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Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024