ORPHA:98657
OBSOLETE: Genetic vitreous-retinal disease
inactive · referred to ORPHA:519315Rare 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 retinal disorder
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Genetic vitreous-retinal disease | |
| fr | OBSOLETE : Maladie génétique de la rétine et du vitré | |
| de | OBSOLET: Vitreoretinale Krankheit, genetisch bedingte | |
| es | OBSOLETO: Enfermedad vitreorretiniana genética | |
| it | OBSOLETO: Malattia vitreo-retinica | |
| nl | OBSOLEET: Genetische vitreoretinale ziekte | |
| pt | OBSOLETO: Doença vítreo-retiniana | |
| pl | NIEAKTUALNE: Genetyczna choroba witreoretinalna | |
| cs | NEAKTUÁLNÍ: Geneticky podmíněné vitreoretinální choroby | |
| uk | ЗАСТАРІЛО: Генетично обумовлене захворювання скловидного тіла та сітківки | |
| zh | 弃用：遗传性玻璃质-视网膜疾病 | |
| tr | Eski adı: Genetik vitreus(vitröz)-retina hastalığı |
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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/98657
- This record as JSON: /data/d/98657.json