ORPHA:71291
Hereditary vascular retinopathy
inactive · moved to ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
Synonyms: HVR · Hereditary vascular retinopathy-Raynaud phenomenon-migraine syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hereditary vascular retinopathy | HVR · Hereditary vascular retinopathy-Raynaud phenomenon-migraine syndrome |
| fr | Rétinopathie vasculaire héréditaire | HVR · RVH · Syndrome de rétinopathie vasculaire héréditaire-phénomène de Raynaud-migraine |
| de | Retinopathie, hereditäre vaskuläre | HVR |
| es | Retinopatía hereditaria vascular | Retinopatía hereditaria vascular-fenómeno de Raynaud-migraña |
| it | Retinopatia vascolare ereditaria | HVR · Retinopatia vascolare ereditaria - fenomeno di Raynaud - emicrania |
| nl | Hereditaire vasculaire retinopathie | Erfelijke vasculaire retinopathie - fenomeen van Raynaud - migraine-syndroom · HVR |
| pt | Retinopatia vascular hereditária | HVR |
| pl | Dziedziczna retinopatia naczyniowa | Dziedziczna retinopatia naczyniowa - fenomen Raynauda - migrena · HVR |
| cs | Hereditární vaskulární retinopatie | HVR · Syndrom zahrnující hereditární vaskulární retinopatii, Raynaudův fenomén a migrénu |
| uk | Спадкова судинна ретинопатія | Синдром спадкової судинної ретинопатії - феномена Рейно - мігрені · HVR |
| zh | 遗传性血管源性视网膜病 | 遗传性血管源性视网膜病-Raynaud现象-偏头痛综合征 |
| tr | Kalıtsal vasküler retinopati | HVR · Kalıtsal vasküler retinopati-Raynaud fenomeni-migren sendromu |
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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/71291
- This record as JSON: /data/d/71291.json