ORPHA:519325
OBSOLETE: Syndromic inherited retinal disorder
inactive · referred to ORPHA:522572Rare genetic retinal disorder
Synonyms: OBSOLETE: Syndromic 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: Syndromic inherited retinal disorder | OBSOLETE: Syndromic retinal dystrophy |
| fr | OBSOLETE : Maladie rétinienne héréditaire syndromique | |
| de | OBSOLET: Syndromale hereditäre retinale Störung | OBSOLET: Netzhautdystrophie, syndromale · OBSOLET: Syndromale Netzhautdystrophie |
| es | OBSOLETO: Trastorno retiniano hereditario sindrómico | OBSOLETO: Distrofia retiniana sindrómica |
| it | OBSOLETO: Patologia retinica sindromica ereditaria | OBSOLETO: Distrofia retinica sindromica |
| nl | OBSOLEET: Syndromale erfelijke aandoening van retina | NIET ZELDZAME ZIEKTE IN EUROPA: Syndromale retinale dystrofie · NIET ZELDZAME ZIEKTE IN EUROPA: Syndromale erfelijke aandoening van netvlies |
| pt | OBSOLETO: Doença retiniana hereditária sindromática | |
| pl | NIEAKTUALNE: Dziedziczna syndromiczna choroba siatkówki | NIEAKTUALNE: Zespół dystrofii siatkówki |
| cs | NEAKTUÁLNÍ: Syndromická dědičná porucha sítnice | NEAKTUÁLNÍ: Syndromická dystrofie sítnice |
| uk | Синдромне спадкове захворювання сітківки | Синдромальна дистрофія сітківки |
| zh | 综合征性遗传性视网膜病变 | 综合性视网膜营养不良 |
| tr | Sendromik kalıtsal retina bozukluğu | Sendromik 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/519325
- This record as JSON: /data/d/519325.json