ORPHA:63261
HERNS syndrome
inactive · moved to ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
Synonyms: Hereditary endotheliopathy-retinopathy-nephropathy-stroke syndrome
- Type
- Malformation syndrome
- 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 | HERNS syndrome | Hereditary endotheliopathy-retinopathy-nephropathy-stroke syndrome |
| fr | HERNS syndrome | Syndrome d'endothéliopathie héréditaire-rétinopathie-néphropathie-crises |
| de | HERNS-Syndrom | Hereditäre Endotheliopathie - Retinopathie - Nephropathie - Schlaganfall |
| es | Síndrome HERNS | |
| it | Sindrome HERNS | Endoteliopatia ereditaria - retinopatia - nefropatia - infarto |
| nl | HERNS-syndroom | Erfelijke endotheliopathie - retinopathie - nefropathie - cerebrovasculair accident-syndroom |
| pt | Síndrome HERNS | Síndrome de endoteliopatia hereditária-retinopatia-nefropatia-AVC |
| pl | Zespół HERNS | Dziedziczna endoteliopatia - retinopatia - nefropatia - udar |
| cs | HERNS syndrom | Syndrom zahrnující hereditární endoteliopatii, retinopatii, nefropatii a mozkovou příhodu |
| uk | Синдром HERNS | Спадковий синдром ендотеліопатії-ретинопатії-нефропатії-інсульту |
| zh | HERNS综合征 | 遗传性血管内皮细胞病-视网膜病-肾病-卒中综合征 |
| tr | HERNS sendromu | Kalıtsal endotelyopati-retinopati-nefropati-inme 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/63261
- This record as JSON: /data/d/63261.json