ORPHA:716441
Rare isolated 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.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare isolated progressive vitreoretinopathy | |
| fr | Vitréorétinopathie isolée progressive rare | |
| de | Seltene isolierte progrediente Vitreoretinopathie | |
| es | Vitreorretinopatía progresiva aislada rara | |
| it | Vitreoretinopatia progressiva isolata rara | |
| nl | Zeldzame geïsoleerde progressieve vitreoretinopathie | |
| pt | Vitréorétinopathie isolée non-progressive rare | |
| pl | Rzadka izolowana postępująca witreoretinopatia | |
| cs | Rare isolated progressive vitreoretinopathy |
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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:716438Rare progressive vitreoretinopathy
rare genetic diseases; rare ophthalmic disorders
Children (6):
4
Genes
0 directOrphanet records no gene directly on this code.
5
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/716441
- This record as JSON: /data/d/716441.json