ORPHA:519319
OBSOLETE: Isolated stationary inherited retinal disorder
inactive · referred to ORPHA:522572Rare genetic retinal disorder
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare genetic retinal disorder
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Isolated stationary inherited retinal disorder | |
| fr | OBSOLETE : Maladie rétinienne héréditaire stationnaire isolée | |
| de | OBSOLET: Isolierte stationäre hereditäre retinale Störung | |
| es | OBSOLETO: Trastorno retiniano hereditario estacionario aislado | |
| it | OBSOLETO: Patologia retinica ereditaria isolata non-progressiva | |
| nl | OBSOLEET: Geïsoleerde stationaire erfelijke aandoening van retina | NIET ZELDZAME ZIEKTE IN EUROPA: Geïsoleerde stationaire erfelijke aandoening van netvlies |
| pt | OBSOLETO: Doença retiniana não-progressiva isolada hereditária | |
| pl | NIEAKTUALNE: Izolowana stacjonarna dziedziczna choroba siatkówki | |
| cs | NEAKTUÁLNÍ: Izolovaná stacionární dědičná porucha sítnice | |
| uk | Ізольоване стаціонарне спадкове захворювання сітківки | |
| zh | 孤立静止性遗传性视网膜病变 | |
| tr | İzole sabit kalıtsal retina bozukluğu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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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/519319
- This record as JSON: /data/d/519319.json