ORPHA:300337
OBSOLETE: Congenital blindness due to retinal non-attachment
inactive · referred to ORPHA:91495Persistent hyperplastic primary vitreous
- 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 Persistent hyperplastic primary vitreous
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Congenital blindness due to retinal non-attachment | |
| fr | OBSOLETE : Cécité congénitale par non-attachement de la rétine | |
| de | OBSOLET: Kongenitale Blindheit durch retinales 'non-attachment' | OBSOLET: Angeborene Blindheit durch Nicht-Anheftung der Netzhaut · OBSOLET: NCRNA-Krankheit · OBSOLET: Netzhautablösung, kongenitale |
| es | OBSOLETO: Ceguera congénita por falta de adhesión de la retina | |
| it | OBSOLETO: Cecità congenita da distacco della retina | OBSOLETO: Distacco retinico congenito · OBSOLETO: Distacco retinico congenito non sindromico · OBSOLETO: Malattia NCRNA |
| nl | OBSOLEET: Congenitale blindheid door niet-aangehechte retina | OBSOLEET: Congenitale niet-aangehechte retina · OBSOLEET: NCRNA-ziekte · OBSOLEET: Niet-syndromaal congenitaal niet-aangehechte retina |
| pt | OBSOLETO: Cegueira congénita devido à não aderência da retina | |
| pl | NIEAKTUALNE: Slepota wrodzona spowodowana odwarstwieniem siatkówki | |
| cs | NEAKTUÁLNÍ: Vrozená slepota způsobená odchlípením sítnice | NEAKTUÁLNÍ: Vrozené odchlípení sítnice · NEAKTUÁLNÍ: Nesyndromické vrozené odchlípení sítnice · NEAKTUÁLNÍ: NCRNA onemocnění |
| uk | ЗАСТАРІЛО: Вроджена сліпота через незрощення сітківки | |
| zh | 弃用：因视网膜未附着而致先天失明 | |
| tr | Eski adı: Retinanın yapışmamasına bağlı doğumsal körlük |
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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/300337
- This record as JSON: /data/d/300337.json