ORPHA:716348
Rare isolated progressive 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 isolated progressive predominantly chorioretinal disorder | |
| fr | Maladie isolée avec atteinte progressive prédominante de la choroïde et de la rétine | |
| de | Seltene isolierte progrediente chorioretinale Störung | |
| es | Trastorno raro predominantemente coriorretiniano progresivo aislado | |
| it | Malattia rara isolata progressiva a predominanza corioretinica | |
| nl | Zeldzame geïsoleerde progressieve aandoening van voornamelijk choroidea en/of retina | Zeldzame geïsoleerde progressieve aandoening van voornamelijk vaatvlies en/of netvlies · Zeldzame geïsoleerde progressieve overwegend chorioretinale aandoening |
| pt | Rare isolated progressive predominantly chorioretinal disorder | |
| pl | Rzadkie izolowane postępujące zaburzenie dotyczące głównie naczyniówki i siatkówki | |
| cs | Rare isolated progressive 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:716304Rare progressive predominantly chorioretinal disorder
rare ophthalmic disorders
Children (9):
- ORPHA:41751Bietti crystalline dystrophy
- ORPHA:85128Bothnia retinal dystrophy
- ORPHA:165958Cavitary myiasis
- ORPHA:443079Central serous chorioretinopathy
- ORPHA:180Choroideremia
- ORPHA:414Gyrate atrophy of choroid and retina
- ORPHA:86813Helicoid peripapillary chorioretinal degeneration
- ORPHA:75373Progressive bifocal chorioretinal atrophy
- ORPHA:35686Serpiginous choroiditis
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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/716348
- This record as JSON: /data/d/716348.json