ORPHA:730393
Genetic isolated posterior fossa cystic malformation
- 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
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic isolated posterior fossa cystic malformation | |
| fr | Malformation kystique génétique isolée de la fosse postérieure | |
| de | Isolierte zystische Fehlbildung der hinteren Schädelgrube, genetisch bedingte | |
| es | Malformación quística genética aislada de la fosa posterior | |
| it | Malformazione cistica isolata genetica della fossa posteriore | |
| nl | Genetische geïsoleerde cysteuze malformatie van fossa cranialis posterior | Genetische geïsoleerde cysteuze malformatie van achterste schedelgroeve |
| pt | Genetic isolated posterior fossa cystic malformation | |
| pl | Genetic isolated posterior fossa cystic malformation | |
| cs | Genetic isolated posterior fossa cystic malformation |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:730390Genetic posterior fossa cystic malformation
rare genetic diseases
Children (1):
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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/730393
- This record as JSON: /data/d/730393.json