ORPHA:730699
Genetic syndromic rhombencephalosynapsis
- 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.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic syndromic rhombencephalosynapsis | |
| fr | Rhombencéphalosynapsis syndromique génétique | |
| de | Syndromale Rhombenzephalosynapsis, genetisch bedingte | |
| es | Rombencefalosinapsis sindrómica genética | |
| it | Rombencefalosinapsi sindromica genetica | |
| nl | Genetische syndromale rombencefalosynapsis | |
| pt | Genetic syndromic rhombencephalosynapsis | |
| pl | Genetic syndromic rhombencephalosynapsis | |
| cs | Genetic syndromic rhombencephalosynapsis |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:269567Genetic syndrome with a cerebellar malformation as a major feature
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/730699
- This record as JSON: /data/d/730699.json