ORPHA:717257
Rare genetic predominantly chorioretinal disorder
- 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 genetic predominantly chorioretinal disorder | |
| fr | Maladie génétique rare avec atteinte prédominante de la choroïde et de la rétine | |
| de | Seltene genetische chorioretinale Störung | |
| es | Trastorno genético raro predominantemente coriorretiniano | |
| it | Malattia genetica rara a predominanza corioretinica | |
| nl | Zeldzame genetische aandoening van voornamelijk choroidea en/of retina | Zeldzame genetische aandoening van voornamelijk vaatvlies en/of netvlies · Zeldzame genetische overwegend chorioretinale aandoening |
| pt | Rare genetic predominantly chorioretinal disorder | |
| pl | Rzadkie genetycznie uwarunkowane zaburzenie siatkówki i naczyniówki | |
| cs | Rare genetic predominantly chorioretinal disorder |
2
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:522572Rare genetic retinal disorder
rare genetic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
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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/717257
- This record as JSON: /data/d/717257.json