{"orpha":71291,"name":"Hereditary vascular retinopathy","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["HVR","Hereditary vascular retinopathy-Raynaud phenomenon-migraine syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations","url":"https://raremap.alftech.space/d/ORPHA-71291/","orphanet_url":"https://www.orpha.net/en/disease/detail/71291","names":{"fr":{"name":"Rétinopathie vasculaire héréditaire","synonyms":["HVR","RVH","Syndrome de rétinopathie vasculaire héréditaire-phénomène de Raynaud-migraine"]},"de":{"name":"Retinopathie, hereditäre vaskuläre","synonyms":["HVR"]},"es":{"name":"Retinopatía hereditaria vascular","synonyms":["Retinopatía hereditaria vascular-fenómeno de Raynaud-migraña"]},"it":{"name":"Retinopatia vascolare ereditaria","synonyms":["HVR","Retinopatia vascolare ereditaria - fenomeno di Raynaud - emicrania"]},"nl":{"name":"Hereditaire vasculaire retinopathie","synonyms":["Erfelijke vasculaire retinopathie - fenomeen van Raynaud - migraine-syndroom","HVR"]},"pt":{"name":"Retinopatia vascular hereditária","synonyms":["HVR"]},"pl":{"name":"Dziedziczna retinopatia naczyniowa","synonyms":["Dziedziczna retinopatia naczyniowa - fenomen Raynauda - migrena","HVR"]},"cs":{"name":"Hereditární vaskulární retinopatie","synonyms":["HVR","Syndrom zahrnující hereditární vaskulární retinopatii, Raynaudův fenomén a migrénu"]},"uk":{"name":"Спадкова судинна ретинопатія","synonyms":["Синдром спадкової судинної ретинопатії - феномена Рейно - мігрені","HVR"]},"zh":{"name":"遗传性血管源性视网膜病","synonyms":["遗传性血管源性视网膜病-Raynaud现象-偏头痛综合征"]},"tr":{"name":"Kalıtsal vasküler retinopati","synonyms":["HVR","Kalıtsal vasküler retinopati-Raynaud fenomeni-migren sendromu"]}},"xrefs":[],"associations":[{"type":"Moved to","orpha":247691,"name":"Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}