ORPHA:108991
OBSOLETE: Syndrome with a central nervous system malformation as a major feature
inactive · referred to ORPHA:98044Central nervous system malformation
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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/>Instead, consider using Central nervous system malformation
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Syndrome with a central nervous system malformation as a major feature | |
| fr | OBSOLETE : Syndrome avec malformation du système nerveux central comme manifestation majeure | |
| de | OBSOLET: Syndrom mit ZNS-Fehlbildung als Hauptmerkmal | |
| es | OBSOLETO: Síndrome con malformación del sistema nervioso central como característica principal | |
| it | OBSOLETO: Sindrome con malformazione del sistema nervoso centrale come segno cardinale | |
| nl | OBSOLEET: Syndroom met malformatie van centraal zenuwstelsel als hoofdkenmerk | |
| pt | OBSOLETO: Síndrome com malformação do sistema nervoso central como característica principal | |
| pl | NIEAKTUALNE: Zespół z malformacją centralnego układu nerwowego jako głównym objawem | |
| cs | NEAKTUÁLNÍ: Syndromy s malformací centrálního nervového systému jako hlavním příznakem | |
| uk | Синдром з ураженням центральної нервової системи як основною ознакою | |
| zh | 以中枢神经系统畸形为主要特征的综合征 | |
| tr | Esas klinik özelliği merkezi sinir sistemi malformasyonu olan sendrom |
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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/108991
- This record as JSON: /data/d/108991.json