ORPHA:269550
OBSOLETE: Genetic non-syndromic central nervous system malformation
inactive · referred to ORPHA:183506Genetic central 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 Genetic central nervous system malformation
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Genetic non-syndromic central nervous system malformation | |
| fr | OBSOLETE : Malformation non syndromique génétique du système nerveux central | |
| de | OBSOLET: Nicht-syndromale Fehlbildung des Zentralnervensystems, genetisch bedingte | |
| es | OBSOLETO: Malformación genética no sindrómica del sistema nervioso central | |
| it | OBSOLETO: Malformazione non sindromica genetica del sistema nervoso centrale | |
| nl | OBSOLEET: Genetische niet-syndromale malformatie van centraal zenuwstelsel | |
| pt | OBSOLETO: Malformação não sindromática do sistema nervoso central genética | |
| pl | NIEAKTUALNE: Niesyndromiczna malformacja centralnego układu nerwowego uwarunkowana genetycznie | |
| cs | NEAKTUÁLNÍ: Geneticky podmíněné nesyndromické malformace centrálního nervového systému | |
| uk | Генетично обумовлена несиндромальна вада розвитку центральної нервової системи | |
| zh | 遗传性非综合征性中枢神经系统畸形 | |
| tr | Genetik sendromik olmayan merkezi sinir sistemi malformasyonu |
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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/269550
- This record as JSON: /data/d/269550.json