ORPHA:1852
OBSOLETE: X-linked retinal dysplasia
inactive · referred to ORPHA:649Norrie disease
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Norrie disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: X-linked retinal dysplasia | |
| fr | OBSOLETE : Dysplasie rétinienne liée à l'X | |
| de | OBSOLET: Retinadysplasie, X-chromosomale | |
| es | OBSOLETO: Displasia retiniana ligada al cromosoma X | |
| it | OBSOLETO: Displasia retinica legata all'X | |
| nl | OBSOLEET: X-gebonden retinale dysplasie | NIET ZELDZAME ZIEKTE IN EUROPA: X-gebonden retinadysplasie · NIET ZELDZAME ZIEKTE IN EUROPA: X-gebonden dysplasie van netvlies |
| pt | OBSOLETO: Displasia da retina ligada ao X | OBSOLETO: Retinopatia ligada ao X |
| pl | NIEAKTUALNE: Dysplazja siatkówki sprzężona z chromosomem X | |
| cs | NEAKTUÁLNÍ: X-vázaná retinální dysplázie | |
| uk | Х-зчеплена дисплазія сітківки | |
| zh | X连锁视网膜发育不良 | |
| tr | X'e bağlı retina displazisi |
Definition in:
2
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/1852
- This record as JSON: /data/d/1852.json