{"id":19754,"date":"2026-06-05T18:22:47","date_gmt":"2026-06-05T16:22:47","guid":{"rendered":"https:\/\/www.cutislaxa.org\/?p=19754"},"modified":"2026-10-02T18:26:22","modified_gmt":"2026-10-02T16:26:22","slug":"orphanet-en-chiffres","status":"publish","type":"post","link":"https:\/\/www.cutislaxa.org\/fr\/orphanet-en-chiffres\/","title":{"rendered":"Orphanet en Chiffres"},"content":{"rendered":"<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-16035 aligncenter\" src=\"https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Logo-Orphanews.jpg\" alt=\"\" width=\"163\" height=\"48\" \/><\/p>\n<p style=\"text-align: center;\"><strong>\u00a0Orphanet\u00a0<\/strong>C\u2019est un r\u00e9seau qui s\u2019\u00e9tend sur <strong>40 pays<\/strong> en Europe et au-del\u00e0.<\/p>\n<p style=\"text-align: center;\">Le site est accessible gratuitement en <strong>9 langues,<\/strong><\/p>\n<p style=\"text-align: center;\"><strong>28 millions de pages<\/strong> ont \u00e9t\u00e9 visit\u00e9es en 2025<strong>,<\/strong><\/p>\n<p style=\"text-align: center;\"><strong>6,622 maladies rares<\/strong> avec un identifiant unique : ORPHA Code,<\/p>\n<p style=\"text-align: center;\"><strong>25,883 professonnels de sant\u00e9<\/strong> r\u00e9f\u00e9renc\u00e9s,<\/p>\n<p style=\"text-align: center;\"><strong>2,798 associations de patients<\/strong> et <strong>31 Alliances Nationales<\/strong> de maladies rares,<\/p>\n<p style=\"text-align: center;\"><strong>8,512 Centres experts, <\/strong><\/p>\n<p style=\"text-align: center;\"><strong>31,742 Tests Diagnostics<\/strong>,<\/p>\n<p style=\"text-align: center;\"><strong>5,605 Registres de patients<\/strong>,<\/p>\n<p style=\"text-align: center;\"><strong>181 biobanques , <\/strong><\/p>\n<p style=\"text-align: center;\"><strong>1,013 laboratoires m\u00e9dicaux d\u00e9di\u00e9s au diagnostic<\/strong>, \u2026..<\/p>\n<p style=\"text-align: center;\">et tellement d\u2019autres ressources\u2026.<\/p>\n<p style=\"text-align: center;\"><a href=\"https:\/\/www.orpha.net\/\">https:\/\/www.orpha.net\/<\/a><\/p>\n<p style=\"text-align: center;\">(\u00a9Orphanews 2026.06.03)<\/p>\n","protected":false},"excerpt":{"rendered":"<p>\u00a0Orphanet\u00a0C\u2019est un r\u00e9seau qui s\u2019\u00e9tend sur 40 pays en Europe et au-del\u00e0. Le site est accessible gratuitement en 9 langues, 28 millions de pages ont \u00e9t\u00e9 visit\u00e9es en 2025, 6,622 maladies rares avec un identifiant unique : ORPHA Code, 25,883 professonnels de sant\u00e9 r\u00e9f\u00e9renc\u00e9s, 2,798 associations de patients et 31 Alliances Nationales de maladies rares, [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":16517,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[61,60,66],"tags":[],"class_list":["post-19754","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-quoi-de-neuf","category-recherche","category-recherche-medecine-genetique"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Orphanet en Chiffres - CUTIS LAXA INTERNATIONALE<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.cutislaxa.org\/fr\/orphanet-en-chiffres\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Orphanet en Chiffres - CUTIS LAXA INTERNATIONALE\" \/>\n<meta property=\"og:description\" content=\"\u00a0Orphanet\u00a0C\u2019est un r\u00e9seau qui s\u2019\u00e9tend sur 40 pays en Europe et au-del\u00e0. 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