ORPHA:166475
Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes | |
| fr | Syndrome épileptique familial idiopathique ou cryptogénique avec gènes/loci identifiés | |
| de | Familiäres Epilepsiesyndrom, idiopathisches oder kryptogenes, mit bekanntem Gen/-ort | |
| es | Síndrome epiléptico familiar idiopático o criptogénico con genes/loci identificados | |
| it | Sindrome epilettica familiare idiopatica o criptogenetica con geni/loci identificati | |
| nl | Idiopathisch of cryptogeen familiaal epileptisch syndroom met geïdentificeerde loci/genen | |
| pt | Síndrome epiléptico familiar, idiopático ou criptogénico, com locus/gene identificado | |
| pl | Idiopatyczny lub kryptogenny rodzinny zespół padaczkowy ze zidentyfikowanym loci/genem | |
| cs | Syndromy idiopatické nebo kryptogenní dědičné epilepsie s identifikovanými lokusy/geny | |
| uk | Ідіопатичний або криптогенний синдром сімейної епілепсії з ідентифікованими локусами/генами | |
| zh | 特发性或隐源性家族性癫痫综合征伴已知位点/基因 | |
| tr | Tanımlanmış lokus / genler ile seyreden idiyopatik veya kriptojenik ailesel epilepsi sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15654 | E | validated | |
| UMLS | C5680431 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:101998Rare epilepsy
rare neurological diseases - ORPHA:183512Rare genetic epilepsy
rare genetic diseases
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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/166475
- This record as JSON: /data/d/166475.json