ORPHA:730707
Genetic forebrain 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 forebrain malformation | |
| fr | Malformation du prosencéphale génétique | |
| de | Fehlbildung des Prosencephalon, genetische bedingte | |
| es | Malformación genética del prosencéfalo | |
| it | Malformazione genetica del proencefalo | |
| nl | Genetische malformatie van voorhersenen | |
| pt | Genetic forebrain malformation | |
| pl | Genetic forebrain malformation | |
| cs | Genetic forebrain malformation |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:183506Genetic central nervous system malformation
rare genetic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/730707
- This record as JSON: /data/d/730707.json