ORPHA:693802
Neonatal/infantile-onset epilepsy syndrome
- Type
- Clinical group
- 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.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neonatal/infantile-onset epilepsy syndrome | |
| fr | Syndrome épileptique du nouveau-né et du nourrisson | |
| de | Epilepsie-Syndrom, neonatales/infantiles | |
| es | Síndrome de epilepsia de inicio neonatal/infantil | |
| it | Sindrome epilettica a esordio neonatale/infantile | |
| nl | Neonataal/infantiel optredend epilepsiesyndroom | |
| pt | Síndrome epilético de início neonatal-infantil | |
| pl | Padaczka o początku w okresie noworodkowym - niemowlęcym | |
| cs | Neonatal/infantile-onset epilepsy syndrome |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:166463Epilepsy syndrome
rare genetic diseases; rare neurological diseases
Children (22):
- ORPHA:505652CDKL5-deficiency disorder
- ORPHA:163681CNTNAP2-related developmental and epileptic encephalopathy
- ORPHA:71277Classic glucose transporter type 1 deficiency syndrome
- ORPHA:33069Dravet syndrome
- ORPHA:1934Early infantile developmental and epileptic encephalopathy
- ORPHA:1943Early-onset progressive encephalopathy with migrant continuous myoclonus
- ORPHA:293181Epilepsy of infancy with migrating focal seizures
- ORPHA:86906Gelastic seizures with hypothalamic hamartoma
- ORPHA:36387Genetic epilepsy with febrile seizure plus
- ORPHA:697160Infantile epileptic spasms syndrome
- ORPHA:439218KCNQ2-related developmental and epileptic encephalopathy
- ORPHA:209370MECP2-related severe neonatal encephalopathy
- ORPHA:86909Myoclonic epilepsy of infancy
- ORPHA:714652PCDH19 clustering epilepsy
- ORPHA:79096Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy
- ORPHA:3006Pyridoxine-dependent-developmental and epileptic encephalopathy
- ORPHA:599373STXBP1-related developmental and epileptic encephalopathy
- ORPHA:544254SYNGAP1-related developmental and epileptic encephalopathy
- ORPHA:306Self-limited infantile epilepsy
- ORPHA:1949Self-limited neonatal epilepsy
- ORPHA:140927Self-limited neonatal/infantile epilepsy
- ORPHA:3205Sturge-Weber syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:86913OBSOLETE: Myoclonic epilepsy in non-progressive encephalopathies referred to · inactive
- ORPHA:98257OBSOLETE: Neonatal epilepsy syndrome referred to · inactive
- ORPHA:98258OBSOLETE: Infantile epilepsy syndrome referred to · inactive
- ORPHA:166305OBSOLETE: Benign infantile seizures associated with mild gastroenteritis referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/693802
- This record as JSON: /data/d/693802.json