Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Jackson–Weiss_syndrome> ?p ?o }
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- Jackson–Weiss_syndrome abstract "Jackson–Weiss syndrome (JWS) is a genetic disorder characterized by foot abnormalities and the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. It can also sometimes cause intellectual disability and crossed eyes as well.It was characterized in 1976.".
- Jackson–Weiss_syndrome omim "123150".
- Jackson–Weiss_syndrome wikiPageExternalLink br.fcgi?book=gene&part=craniosynostosis.
- Jackson–Weiss_syndrome wikiPageID "3443488".
- Jackson–Weiss_syndrome wikiPageLength "4257".
- Jackson–Weiss_syndrome wikiPageOutDegree "17".
- Jackson–Weiss_syndrome wikiPageRevisionID "706869318".
- Jackson–Weiss_syndrome wikiPageWikiLink Category:Autosomal_dominant_disorders.
- Jackson–Weiss_syndrome wikiPageWikiLink Category:Cell_surface_receptor_deficiencies.
- Jackson–Weiss_syndrome wikiPageWikiLink Category:Rare_diseases.
- Jackson–Weiss_syndrome wikiPageWikiLink Category:Syndromes.
- Jackson–Weiss_syndrome wikiPageWikiLink Craniosynostosis.
- Jackson–Weiss_syndrome wikiPageWikiLink Dominance_(genetics).
- Jackson–Weiss_syndrome wikiPageWikiLink Embryo.
- Jackson–Weiss_syndrome wikiPageWikiLink Esotropia.
- Jackson–Weiss_syndrome wikiPageWikiLink Fetus.
- Jackson–Weiss_syndrome wikiPageWikiLink Fibroblast_growth_factor_receptor_2.
- Jackson–Weiss_syndrome wikiPageWikiLink Gene.
- Jackson–Weiss_syndrome wikiPageWikiLink Genetic_disorder.
- Jackson–Weiss_syndrome wikiPageWikiLink Intellectual_disability.
- Jackson–Weiss_syndrome wikiPageWikiLink Mutation.
- Jackson–Weiss_syndrome wikiPageWikiLink Protein.
- Jackson–Weiss_syndrome wikiPageWikiLink File:Autosomal_dominant_-_en.svg.
- Jackson–Weiss_syndrome wikiPageWikiLinkText "Jackson–Weiss syndrome ".
- Jackson–Weiss_syndrome wikiPageWikiLinkText "Jackson–Weiss syndrome".
- Jackson–Weiss_syndrome diseasesdb "31364".
- Jackson–Weiss_syndrome name "Jackson–Weiss syndrome".
- Jackson–Weiss_syndrome omim "123150".
- Jackson–Weiss_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Jackson–Weiss_syndrome wikiPageUsesTemplate Template:Receptor_deficiencies.
- Jackson–Weiss_syndrome wikiPageUsesTemplate Template:Reflist.
- Jackson–Weiss_syndrome subject Category:Autosomal_dominant_disorders.
- Jackson–Weiss_syndrome subject Category:Cell_surface_receptor_deficiencies.
- Jackson–Weiss_syndrome subject Category:Rare_diseases.
- Jackson–Weiss_syndrome subject Category:Syndromes.
- Jackson–Weiss_syndrome hypernym Disorder.
- Jackson–Weiss_syndrome type Disease.
- Jackson–Weiss_syndrome type Deficiency.
- Jackson–Weiss_syndrome type Disorder.
- Jackson–Weiss_syndrome type Redirect.
- Jackson–Weiss_syndrome type Syndrome.
- Jackson–Weiss_syndrome type Thing.
- Jackson–Weiss_syndrome type Q12136.
- Jackson–Weiss_syndrome comment "Jackson–Weiss syndrome (JWS) is a genetic disorder characterized by foot abnormalities and the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. It can also sometimes cause intellectual disability and crossed eyes as well.It was characterized in 1976.".
- Jackson–Weiss_syndrome label "Jackson–Weiss syndrome".
- Jackson–Weiss_syndrome sameAs Q6118062.
- Jackson–Weiss_syndrome sameAs Jackson-Weiss-Syndrom.
- Jackson–Weiss_syndrome sameAs Zespół_Jacksona-Weissa.
- Jackson–Weiss_syndrome sameAs m.09cq8n.
- Jackson–Weiss_syndrome sameAs Q6118062.
- Jackson–Weiss_syndrome wasDerivedFrom Jackson–Weiss_syndrome?oldid=706869318.
- Jackson–Weiss_syndrome isPrimaryTopicOf Jackson–Weiss_syndrome.
- Jackson–Weiss_syndrome name "Jackson–Weiss syndrome".