{"id":92,"date":"2017-08-29T02:18:00","date_gmt":"2017-08-29T02:18:00","guid":{"rendered":"https:\/\/lab.research.sickkids.ca\/cangard\/?page_id=92"},"modified":"2019-10-17T21:00:32","modified_gmt":"2019-10-17T21:00:32","slug":"resources","status":"publish","type":"page","link":"https:\/\/lab.research.sickkids.ca\/cangard\/resources\/","title":{"rendered":"Resources"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row][vc_column][vc_column_text]<a href=\"http:\/\/care4rare.ca\" target=\"_blank\" rel=\"noopener\">CARE for RARE<\/a><\/p>\n<p><a href=\"https:\/\/www.raredisorders.ca\" target=\"_blank\" rel=\"noopener\">Canadian Organization for Rare Disorders<\/a><\/p>\n<p><a href=\"https:\/\/www.rarediseasefoundation.org\" target=\"_blank\" rel=\"noopener\">Rare Disease Foundation<\/a><\/p>\n<p><a href=\"https:\/\/rarediseases.org\" target=\"_blank\" rel=\"noopener\">National Organization for Rare Disorders (NORD)<\/a><\/p>\n<p><a href=\"https:\/\/rarediseases.info.nih.gov\" target=\"_blank\" rel=\"noopener\">Genetics and Rare Disease Information Center (GARD)<\/a><\/p>\n<p><a href=\"http:\/\/www.eurordis.org\/about-eurordis\" target=\"_blank\" rel=\"noopener\">EURODIS Rare Disease Europe<\/a><\/p>\n<p><a href=\"https:\/\/ec.europa.eu\/health\/rare_diseases\/expert_group_en\" target=\"_blank\" rel=\"noopener\">European Commission Expert Group<\/a> (formerly European Union Committee of Experts on Rare Disease &#8211; EUCERD)[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column]<div id=\"ultimate-heading-468569e04dc07f840\" class=\"uvc-heading ult-adjust-bottom-margin ultimate-heading-468569e04dc07f840 uvc-5852  uvc-heading-default-font-sizes\" data-hspacer=\"no_spacer\"  data-halign=\"center\" style=\"text-align:center\"><div class=\"uvc-heading-spacer no_spacer\" style=\"top\"><\/div><div class=\"uvc-sub-heading ult-responsive\"  data-ultimate-target='.uvc-heading.ultimate-heading-468569e04dc07f840 .uvc-sub-heading '  data-responsive-json-new='{\"font-size\":\"\",\"line-height\":\"\"}'  style=\"font-weight:normal;\"><img loading=\"lazy\" decoding=\"async\" class=\"alignleft size-full wp-image-308\" src=\"https:\/\/lab.research.sickkids.ca\/cangard\/wp-content\/uploads\/sites\/62\/2017\/10\/ce870f6c2a2e9129dcb05f72b8ce9339-wallpapers-for-desktop-desktop-backgrounds.jpg\" alt=\"\" width=\"736\" height=\"204\" \/><\/div><\/div>[\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][vc_column_text]CARE for RARE Canadian Organization for Rare Disorders Rare Disease Foundation National Organization for Rare Disorders (NORD) Genetics and Rare Disease Information Center (GARD) EURODIS Rare Disease Europe European Commission Expert Group (formerly European Union Committee of Experts on Rare Disease &#8211; EUCERD)[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][\/vc_column][\/vc_row]<\/p>\n","protected":false},"author":4,"featured_media":0,"parent":0,"menu_order":6,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-92","page","type-page","status-publish","hentry","description-off"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.0 (Yoast SEO v27.0) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Resources - Can-GARD<\/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:\/\/lab.research.sickkids.ca\/cangard\/resources\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Resources\" \/>\n<meta property=\"og:description\" content=\"[vc_row][vc_column][vc_column_text]CARE for RARE Canadian Organization for Rare Disorders Rare Disease Foundation National Organization for Rare Disorders (NORD) Genetics and Rare Disease Information Center (GARD) EURODIS Rare Disease Europe European Commission Expert Group (formerly European Union Committee of Experts on Rare Disease &#8211; 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