ORPHA:716438
Rare progressive vitreoretinopathy
- 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 | Rare progressive vitreoretinopathy | |
| fr | Vitréorétinopathie progressive rare | |
| de | Seltene progrediente Vitreoretinopathie | |
| es | Vitreorretinopatía progresiva rara | |
| it | Vitreoretinopatia progressiva rara | |
| nl | Zeldzame progressieve vitreoretinopathie | |
| pt | Rare progressive vitreoretinopathy | |
| pl | Rzadka postępująca witroretinopatia | |
| cs | Rare progressive vitreoretinopathy |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98668Vitreoretinopathy
rare genetic diseases; rare ophthalmic disorders
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/716438
- This record as JSON: /data/d/716438.json