Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Allan–Herndon–Dudley_syndrome> ?p ?o }
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- Allan–Herndon–Dudley_syndrome 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.".
- Allan–Herndon–Dudley_syndrome omim "300523".
- Allan–Herndon–Dudley_syndrome wikiPageExternalLink condition=allanherndondudleysyndrome?wf=1.
- Allan–Herndon–Dudley_syndrome wikiPageExternalLink br.fcgi?book=gene&part=thctd.
- Allan–Herndon–Dudley_syndrome wikiPageID "11233375".
- Allan–Herndon–Dudley_syndrome wikiPageLength "6044".
- Allan–Herndon–Dudley_syndrome wikiPageOutDegree "21".
- Allan–Herndon–Dudley_syndrome wikiPageRevisionID "643021395".
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Brain.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Category:Membrane_transport_protein_disorders.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Category:Neurogenetic_disorders.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Contracture.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Gene.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Hypotonia.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Intellectual_disability.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Male.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Monocarboxylate_transporter_8.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Muscle_hypoplasia.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Nerve_cell.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Nervous_system.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Neuron.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink SLC16A2.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Spasticity.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Synapse.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Synapses.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Thyroid.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Tiratricol.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Triiodothyronine.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink Wheelchair.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink William_Allan_(geneticist).
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink X-linked_recessive.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink X-linked_recessive_inheritance.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLink File:X-linked_recessive.svg.
- Allan–Herndon–Dudley_syndrome wikiPageWikiLinkText "Allan–Herndon–Dudley syndrome".
- Allan–Herndon–Dudley_syndrome hasPhotoCollection Allan–Herndon–Dudley_syndrome.
- Allan–Herndon–Dudley_syndrome name "Allan–Herndon–Dudley syndrome".
- Allan–Herndon–Dudley_syndrome omim "300523".
- Allan–Herndon–Dudley_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Allan–Herndon–Dudley_syndrome wikiPageUsesTemplate Template:Solute_carrier_disorders.
- Allan–Herndon–Dudley_syndrome subject Category:Membrane_transport_protein_disorders.
- Allan–Herndon–Dudley_syndrome subject Category:Neurogenetic_disorders.
- Allan–Herndon–Dudley_syndrome type Disease.
- Allan–Herndon–Dudley_syndrome type Thing.
- Allan–Herndon–Dudley_syndrome type Q12136.
- Allan–Herndon–Dudley_syndrome 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).".
- Allan–Herndon–Dudley_syndrome label "Allan–Herndon–Dudley syndrome".
- Allan–Herndon–Dudley_syndrome sameAs Allan-Herndon-Dudley-Syndrom.
- Allan–Herndon–Dudley_syndrome sameAs Allan–Herndonin_oireyhtymä.
- Allan–Herndon–Dudley_syndrome sameAs Sindrome_di_Allan-Herndon-Dudley.
- Allan–Herndon–Dudley_syndrome sameAs m.02r4h__.
- Allan–Herndon–Dudley_syndrome sameAs Q4731121.
- Allan–Herndon–Dudley_syndrome sameAs Q4731121.
- Allan–Herndon–Dudley_syndrome wasDerivedFrom Allan–Herndon–Dudley_syndrome?oldid=643021395.
- Allan–Herndon–Dudley_syndrome isPrimaryTopicOf Allan–Herndon–Dudley_syndrome.
- Allan–Herndon–Dudley_syndrome name "Allan–Herndon–Dudley syndrome".