Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q4731121> ?p ?o }
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- Q4731121 subject Q13276590.
- Q4731121 subject Q8620826.
- Q4731121 abstract "Allan–Herndon–Dudley syndrome is a rare X-linked inherited disorder of brain development that causes moderate to severe intellectual disability and problems with movement. This condition, which occurs almost exclusively in males, disrupts development from before birth.Allan–Herndon–Dudley syndrome, which is named eponymously for William Allan, Florence C. Dudley, and C. Nash Herndon, results from a mutation of the thyroid hormone transporter MCT8 (also referred to as SLC16A2). Consecutively, thyroid hormones are unable to enter the nervous system, which depends on thyroid signaling for proper function and development.".
- Q4731121 omim "300523".
- Q4731121 wikiPageExternalLink condition=allanherndondudleysyndrome?wf=1.
- Q4731121 wikiPageExternalLink br.fcgi?book=gene&part=thctd.
- Q4731121 wikiPageWikiLink Q1073.
- Q4731121 wikiPageWikiLink Q117060.
- Q4731121 wikiPageWikiLink Q13276590.
- Q4731121 wikiPageWikiLink Q1480291.
- Q4731121 wikiPageWikiLink Q16399.
- Q4731121 wikiPageWikiLink Q1753547.
- Q4731121 wikiPageWikiLink Q18031570.
- Q4731121 wikiPageWikiLink Q183560.
- Q4731121 wikiPageWikiLink Q187181.
- Q4731121 wikiPageWikiLink Q191931.
- Q4731121 wikiPageWikiLink Q1988987.
- Q4731121 wikiPageWikiLink Q327362.
- Q4731121 wikiPageWikiLink Q43054.
- Q4731121 wikiPageWikiLink Q44148.
- Q4731121 wikiPageWikiLink Q7187.
- Q4731121 wikiPageWikiLink Q7809151.
- Q4731121 wikiPageWikiLink Q8004328.
- Q4731121 wikiPageWikiLink Q8620826.
- Q4731121 wikiPageWikiLink Q9404.
- Q4731121 name "Allan–Herndon–Dudley syndrome".
- Q4731121 omim "300523".
- Q4731121 type Disease.
- Q4731121 type Thing.
- Q4731121 type Q12136.
- Q4731121 comment "Allan–Herndon–Dudley syndrome is a rare X-linked inherited disorder of brain development that causes moderate to severe intellectual disability and problems with movement. This condition, which occurs almost exclusively in males, disrupts development from before birth.Allan–Herndon–Dudley syndrome, which is named eponymously for William Allan, Florence C. Dudley, and C. Nash Herndon, results from a mutation of the thyroid hormone transporter MCT8 (also referred to as SLC16A2).".
- Q4731121 label "Allan–Herndon–Dudley syndrome".
- Q4731121 name "Allan–Herndon–Dudley syndrome".