ORPHA:716446
Rare disorder with progressive vitreoretinopathy disorder as a major feature
- 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 disorder with progressive vitreoretinopathy disorder as a major feature | |
| fr | Maladie rare avec vitreoretinopathie progressive comme manifestation majeure | |
| de | Seltene Störung mit progredienter Vitreoretinopathie als Hauptmerkmal | |
| es | Trastorno raro con afectación de vitreorretinopatía progresiva como característica principal | |
| it | Malattia rara con vitroretinopatia progressiva come caratteristica principale | |
| nl | Zeldzame aandoening met progressieve vitreoretinopathie als een hoofdkenmerk | |
| pt | Rare disorder with progressive vitreoretinopathy disorder as a major feature | |
| pl | Rzadkie zaburzenie z witreopatią jako dominującą cechą | |
| cs | Rare disorder with progressive vitreoretinopathy disorder as a major feature |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:716438Rare progressive vitreoretinopathy
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/716446
- This record as JSON: /data/d/716446.json