{"id":9047,"date":"2020-10-08T18:32:21","date_gmt":"2020-10-08T22:32:21","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=9047"},"modified":"2024-08-21T03:23:34","modified_gmt":"2024-08-21T07:23:34","slug":"kmt5b","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/kmt5b\/","title":{"rendered":"KMT5B"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The information for this summary of <\/span><strong><span class=\"notranslate\">KMT5B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> comes from research publications. This is not meant to take the place of medical advice.<\/span><\/p>\n<p><a href=\"https:\/\/www.simonssearchlight.org\/gene-guide\/kmt5b\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here for our full KMT5B Gene Guide<\/strong><\/a><\/p>\n<p>The online Gene Guide includes more information about <span class=\"notranslate\">KMT5B<\/span> such as the chance of having another child with this condition, behavior, and development concerns linked to <span class=\"notranslate\">KMT5B<\/span>-related syndrome or specialists to consider for people with this condition. Share this resource with family members or your clinical providers.<\/p>\n<p><strong><span class=\"notranslate\">KMT5B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> is also called <\/span><strong>intellectual developmental disorder, autosomal dominant 51<\/strong><span style=\"font-weight: 400;\">.<\/span> <span style=\"font-weight: 400;\">For this webpage, we will be using the name <\/span><strong><span class=\"notranslate\">KMT5B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> to encompass the wide range of variants observed in the people identified.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The information for this summary of KMT5B-related syndrome comes from research publications. This is not meant to take the place of medical advice. Click here for our full KMT5B Gene Guide The online Gene Guide includes more information about KMT5B such as the chance of having another child with this condition, behavior, and development concerns [&hellip;]<\/p>\n","protected":false},"author":13,"featured_media":0,"parent":29,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-gene-card.php","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"acf":[],"_links":{"self":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/9047"}],"collection":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/users\/13"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=9047"}],"version-history":[{"count":21,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/9047\/revisions"}],"predecessor-version":[{"id":54626,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/9047\/revisions\/54626"}],"up":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/29"}],"wp:attachment":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/media?parent=9047"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}