ORPHA:716393
Rare disorder with non-progressive generalized retinal disorder as a major feature
Synonyms: Rare syndromic non-progressive generalized retinal 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 disorder with non-progressive generalized retinal disorder as a major feature | Rare syndromic non-progressive generalized retinal disorder |
| fr | Maladie rare avec atteinte non-progressive rétinienne généralisée comme manifestation majeure | |
| de | Seltene Störung mit nicht-progredienter generalisierter retinaler Störung als Hauptmerkmal | Seltene syndromale nicht-progrediente generalisierter Retinopathie |
| es | Trastorno raro con afectación retiniana generalizada no progresiva como característica principal | Trastorno retiniano generalizado no progresivo sindrómico raro |
| it | Malattia rara con retinopatia generalizzata non progressiva come caratteristica principale | Retinopatia generalizzata sindromica rara non progressiva |
| nl | Zeldzame aandoening met niet-progressieve gegeneraliseerde aandoening van retina als een hoofdkenmerk | Zeldzame syndromale niet-progressieve gegeneraliseerde aandoening van retina |
| pt | Rare disorder with non-progressive generalized retinal disorder as a major feature | |
| pl | Rzadkie niepostępujące uogólnione zaburzenie z zajęciem siatkówki jako dominującą cechą | = en |
| cs | Rare disorder with non-progressive generalized retinal disorder as a major feature | = en |
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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:716364Rare non-progressive generalized retinal disorder
rare genetic diseases; rare ophthalmic disorders
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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/716393
- This record as JSON: /data/d/716393.json