ORPHA:726812
Self limited focal childhood epilepsy
Synonyms: SFEC
- 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 | Self limited focal childhood epilepsy | SFEC |
| fr | Epilepsie focale autolimitée de l'enfance | = en |
| de | Selbstlimitierende fokale Epilepsie des Kindesalters | = en |
| es | Epilepsia focal autolimitada infantil | |
| it | Epilessia infantile focale autolimitante | = en |
| nl | Zelflimiterende focale epilepsie op kinderleeftijd | SFEC · Zelflimiterende focale epilepsie in de kindertijd |
| pt | Self limited focal childhood epilepsy | |
| pl | Self limited focal childhood epilepsy | = en |
| cs | Self limited focal childhood epilepsy | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98259Childhood-onset epilepsy syndrome
rare genetic diseases; rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
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/726812
- This record as JSON: /data/d/726812.json