ORPHA:98661
OBSOLETE: Syndromic rod-cone dystrophy
inactive · referred to ORPHA:519315Rare retinal disorder
Synonyms: OBSOLETE: Syndromic retinitis pigmentosa
- 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: Syndromic rod-cone dystrophy | OBSOLETE: Syndromic retinitis pigmentosa |
| fr | OBSOLETE : Dystrophie à bâtonnets prédominants syndromique | |
| de | OBSOLET: Zapfen-Stäbchen-Dystrophie, syndromale | |
| es | OBSOLETO: Distrofia sindrómica de conos y bastones | OBSOLETO: Retinosis pigmentaria sindrómica |
| it | OBSOLETO: distrofia sindromica dei coni e dei bastoncelli | OBSOLETO: Retinite pigmentosa sindromica |
| nl | OBSOLEET: Syndromale kegel-staafdystrofie | |
| pt | OBSOLETO: Retinite pigmentosa sindromática | |
| pl | NIEAKTUALNE: Syndromiczna dystrofia czopkowo-pręcikowa | = en |
| cs | NEAKTUÁLNÍ: Syndromy s retinitis pigmentosa | = en |
| uk | Синдромальна стрижнево-конічна дистрофія | Синдром пігментної дегенерації сітківки |
| zh | 综合征性视杆-视锥萎缩 | 综合征性色素沉着性视网膜炎 |
| tr | Sendromik çubuk-koni distrofisi | Sendromik retinitis pigmentosa |
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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/98661
- This record as JSON: /data/d/98661.json