ORPHA:71862
OBSOLETE: Inherited retinal disorder
inactive · referred to ORPHA:522572Rare genetic retinal disorder
Synonyms: OBSOLETE: Retinal dystrophy
- 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: Inherited retinal disorder | OBSOLETE: Retinal dystrophy |
| fr | OBSOLETE : Maladie rétinienne héréditaire | OBSOLETE : Dystrophie rétinienne |
| de | OBSOLET: Vererbte retinale Störung | |
| es | OBSOLETO: Trastorno retiniano hereditario | OBSOLETO: Distrofia retiniana |
| it | OBSOLETO: Disturbo retinico ereditario | OBSOLETO: Distrofia retinica |
| nl | OBSOLEET: Erfelijke aandoening van retina | NIET ZELDZAME ZIEKTE IN EUROPA: Retinadystrofie · NIET ZELDZAME ZIEKTE IN EUROPA: Erfelijke aandoening van netvlies |
| pt | OBSOLETO: Distrofia da retina, genética | |
| pl | NIEAKTUALNE: Dziedziczne zaburzenie siatkówki | = en |
| cs | NEAKTUÁLNÍ: Retinální dystrofie | = en |
| uk | Неспадкова хвороба сітківки | Дистрофія сітківки |
| zh | 遗传性视网膜疾病 | 视网膜营养不良 |
| tr | Kalıtsal retina bozukluğu | Retina distrofisi |
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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/71862
- This record as JSON: /data/d/71862.json