ORPHA:716290
Rare 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 predominantly chorioretinal disorder | |
| fr | Maladie avec atteinte prédominante de la choroïde et de la rétine rare | |
| de | Seltene chorioretinale Störung | |
| es | Trastorno raro predominantemente coriorretiniano | |
| it | Malattia rara a predominanza corioretinica | |
| nl | Zeldzame aandoening van voornamelijk choroidea en/of retina | Zeldzame aandoening van voornamelijk vaatvlies en/of netvlies · Zeldzame overwegend chorioretinale aandoening |
| pt | Rare predominantly chorioretinal disorder | |
| pl | Rzadkie zaburzenie dotyczące głównie naczyniówki i siatkówki | |
| cs | Rare predominantly chorioretinal disorder |
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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:519315Rare retinal disorder
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:519300OBSOLETE: Isolated chorioretinal dystrophy referred to · inactive
- ORPHA:519321OBSOLETE: Syndromic chorioretinal dystrophy referred to · inactive
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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/716290
- This record as JSON: /data/d/716290.json