ORPHA:166295
Benign non-familial infantile seizures
inactive · moved to ORPHA:306Self-limited infantile epilepsy
- Type
- Clinical group
- Group
- Group of disorders
- Status
- inactive
- Flag
- Deprecated entity
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.<br/><br/>This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Self-limited infantile epilepsy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Benign non-familial infantile seizures | |
| fr | Convulsions infantiles bénignes non familiales | |
| de | Krampfanfälle, benigne infantile nicht-familiäre | |
| es | Crisis infantiles no familiares benignas | |
| it | Convulsioni infantili non familiari benigne | |
| nl | Goedaardige niet-familiale infantiele epileptische aanvallen | |
| pt | Convulsões infantis não familiares benignas | |
| pl | Łagodne nierodzinne drgawki niemowlęce | |
| cs | Benigní non-familiární infantilní křeče | |
| uk | Доброякісні несімейні інфантильні судоми | |
| zh | 良性非家族性婴儿惊厥 | |
| tr | Selim ailesel olmayan infantil nöbetler |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015637 | E | validated | |
| UMLS | C5680425 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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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/166295
- This record as JSON: /data/d/166295.json