ORPHA:98259
Childhood-onset epilepsy syndrome
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Childhood-onset epilepsy syndrome | |
| fr | Syndrome épileptique de l'enfance | |
| de | Epilepsie-Syndrom, im Kindesalter beginnend | |
| es | Síndrome de epilepsia de inicio en la infancia | |
| it | Sindrome epilettica ad esordio infantile | |
| nl | Epilepsiesyndroom met aanvang in de kinderjaren | |
| pt | Síndrome epilepsia de início na infância | |
| pl | Zespół padaczkowy okresu | |
| cs | Epileptické syndromy s nástupem v dětství | |
| uk | Синдром дитячої епілепсії | |
| zh | 儿童早发型癫痫综合征 | |
| tr | Çocukluk çağı başlangıçlı epilepsi sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020072 | E | validated | |
| UMLS | C5681526 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:166463Epilepsy syndrome
rare genetic diseases; rare neurological diseases
Children (21):
- ORPHA:363567Acute encephalopathy with inflammation-mediated status epilepticus
- ORPHA:1544Benign focal seizures of adolescence
- ORPHA:64280Childhood absence epilepsy
- ORPHA:163708Cryptogenic late-onset epileptic spasms
- ORPHA:725Developmental and epileptic encephalopathy with spike-wave activation in sleep
- ORPHA:289266Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
- ORPHA:139431Epilepsy with eyelid myoclonia
- ORPHA:86911Epilepsy with myoclonic absences
- ORPHA:1942Epilepsy with myoclonic-atonic seizures
- ORPHA:163717Familial mesial temporal lobe epilepsy
- ORPHA:98819Familial temporal lobe epilepsy
- ORPHA:79137Generalized epilepsy-paroxysmal dyskinesia syndrome
- ORPHA:36387Genetic epilepsy with febrile seizure plus
- ORPHA:86908Hemiconvulsion-hemiplegia-epilepsy syndrome
- ORPHA:98818Landau-Kleffner syndrome
- ORPHA:2382Lennox-Gastaut syndrome
- ORPHA:99701Mesial temporal lobe epilepsy with hippocampal sclerosis
- ORPHA:139426Perioral myoclonia with absences
- ORPHA:163727Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
- ORPHA:163721Rolandic epilepsy-speech dyspraxia syndrome
- ORPHA:726812Self limited focal childhood epilepsy
Codes that Orphanet moved or referred to this one:
- ORPHA:309OBSOLETE: Familial partial epilepsy referred to · inactive
- ORPHA:1167OBSOLETE: Facial asymmetry-temporal seizures syndrome referred to · inactive
- ORPHA:25968OBSOLETE: Self-limited childhood occipital epilepsy referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98259
- This record as JSON: /data/d/98259.json