ORPHA:93951
OBSOLETE: X-linked dominant intellectual disability-epilepsy syndrome
inactive · referred to ORPHA:2076X-linked intellectual disability-epilepsy syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using X-linked intellectual disability-epilepsy syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: X-linked dominant intellectual disability-epilepsy syndrome | |
| fr | OBSOLETE : Epilepsie-déficience intellectuelle dominante liée à l'X | |
| de | OBSOLET: X-chromosomal-dominante Intelligenzminderung-Epilepsie-Syndrom | |
| es | OBSOLETO: Síndrome de discapacidad intelectual ligada al cromosoma X, forma dominante-epilepsia | |
| it | OBSOLETO: Deficit cognitivo - epilessia , tipo dominante legato all'X | |
| nl | OBSOLEET: X-gebonden dominante intellectuele achterstand - epilepsie | |
| pt | OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual ligado ao X dominante-epilepsia | |
| pl | NIEAKTUALNE: Niepelnosprawnosc intelektualna dominujaca sprzezona z chromosomem X - padaczka | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující X-vázanou dominantní mentální retardaci a epilepsii | |
| uk | Зчеплений з Х-хромосомою синдром домінантної інтелектуальної недостатності та епілепсії | |
| zh | 弃用：X连锁显性智力障碍-癫痫综合征 | |
| tr | Eski adı: X'e bağlı dominant zihinsel yetersizlik-epilepsi sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/93951
- This record as JSON: /data/d/93951.json