childhood-onset epilepsy syndrome
MONDO:0020072Mondo
Findings
No curated finding names childhood-onset epilepsy syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A epilepsy syndrome that occurs during childhood.
Definition from the Mondo Disease Ontology (MONDO:0020072), read 2026-09-29. CC BY 4.0.
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.
- KCNT1HGNC:18865
- Definitive · ClinGen · Autosomal dominant · 2022
Where it sits
- A kind of
- Narrower terms (16)
- acute encephalopathy with biphasic seizures and late reduced diffusion
- atypical childhood epilepsy with centrotemporal spikes
- childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy
- childhood-onset genetic generalized epilepsy syndrome
- childhood-onset idiopathic generalized epilepsy syndrome
- childhood-onset self-limited focal epilepsy syndrome
- cryptogenic late-onset epileptic spasms
- early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
- familial partial epilepsy
- Landau-Kleffner syndrome
- new-onset refractory status epilepticus
- perioral myoclonia with absences
- rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
- rolandic epilepsy-speech dyspraxia syndrome
- self-limited childhood occipital epilepsy
- Sunflower syndrome
Other names
4 names
Resolves to: childhood-onset epilepsy syndrome
- Also called
- childhood epilepsy syndromeepilepsy syndrome of childhoodpaediatric epilepsy syndromepediatric epilepsy syndrome