raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enHERNS syndromeHereditary endotheliopathy-retinopathy-nephropathy-stroke syndrome
frHERNS syndromeSyndrome d'endothéliopathie héréditaire-rétinopathie-néphropathie-crises
deHERNS-SyndromHereditäre Endotheliopathie - Retinopathie - Nephropathie - Schlaganfall
esSíndrome HERNS
itSindrome HERNSEndoteliopatia ereditaria - retinopatia - nefropatia - infarto
nlHERNS-syndroomErfelijke endotheliopathie - retinopathie - nefropathie - cerebrovasculair accident-syndroom
ptSíndrome HERNSSíndrome de endoteliopatia hereditária-retinopatia-nefropatia-AVC
plZespół HERNSDziedziczna endoteliopatia - retinopatia - nefropatia - udar
csHERNS syndromSyndrom zahrnující hereditární endoteliopatii, retinopatii, nefropatii a mozkovou příhodu
ukСиндром HERNSСпадковий синдром ендотеліопатії-ретинопатії-нефропатії-інсульту
zhHERNS综合征遗传性血管内皮细胞病-视网膜病-肾病-卒中综合征
trHERNS sendromuKalıtsal endotelyopati-retinopati-nefropati-inme sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card