Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Worth_syndrome> ?p ?o }
Showing triples 1 to 55 of
55
with 100 triples per page.
- Worth_syndrome abstract "Worth syndrome, also known as benign form of Worth hyperostosis corticalis generalisata with torus platinus, autosomal dominant osteosclerosis, autosomal dominant endosteal hyperostosis or Worth disease, is a rare autosomal dominant congenital disorder that is caused by a mutation in the LRP5 gene. It is characterized by increased bone density and benign bony structures on the palate.".
- Worth_syndrome omim "144750".
- Worth_syndrome thumbnail Autosomal_dominant_-_en.svg?width=300.
- Worth_syndrome wikiPageID "22068733".
- Worth_syndrome wikiPageLength "3009".
- Worth_syndrome wikiPageOutDegree "23".
- Worth_syndrome wikiPageRevisionID "679117928".
- Worth_syndrome wikiPageWikiLink Autosome.
- Worth_syndrome wikiPageWikiLink Benignity.
- Worth_syndrome wikiPageWikiLink Bone.
- Worth_syndrome wikiPageWikiLink Category:Autosomal_dominant_disorders.
- Worth_syndrome wikiPageWikiLink Category:Congenital_disorders.
- Worth_syndrome wikiPageWikiLink Category:Rare_diseases.
- Worth_syndrome wikiPageWikiLink Category:Syndromes.
- Worth_syndrome wikiPageWikiLink Chromosome.
- Worth_syndrome wikiPageWikiLink Chromosome_11_(human).
- Worth_syndrome wikiPageWikiLink Congenital_disorder.
- Worth_syndrome wikiPageWikiLink Dominance_(genetics).
- Worth_syndrome wikiPageWikiLink H._M._Worth.
- Worth_syndrome wikiPageWikiLink LRP5.
- Worth_syndrome wikiPageWikiLink Mutation.
- Worth_syndrome wikiPageWikiLink Nerve.
- Worth_syndrome wikiPageWikiLink Palate.
- Worth_syndrome wikiPageWikiLink Physician.
- Worth_syndrome wikiPageWikiLink Sclerostin.
- Worth_syndrome wikiPageWikiLink Spain.
- Worth_syndrome wikiPageWikiLink File:Autosomal_dominant_-_en.svg.
- Worth_syndrome wikiPageWikiLinkText "Worth syndrome".
- Worth_syndrome diseasesdb "32107".
- Worth_syndrome name "Worth syndrome".
- Worth_syndrome omim "144750".
- Worth_syndrome wikiPageUsesTemplate Template:Cell_surface_receptor_deficiencies.
- Worth_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Worth_syndrome wikiPageUsesTemplate Template:Reflist.
- Worth_syndrome subject Category:Autosomal_dominant_disorders.
- Worth_syndrome subject Category:Congenital_disorders.
- Worth_syndrome subject Category:Rare_diseases.
- Worth_syndrome subject Category:Syndromes.
- Worth_syndrome hypernym Disorder.
- Worth_syndrome type Disease.
- Worth_syndrome type Disorder.
- Worth_syndrome type Pediatric.
- Worth_syndrome type Redirect.
- Worth_syndrome type Syndrome.
- Worth_syndrome type Thing.
- Worth_syndrome type Q12136.
- Worth_syndrome comment "Worth syndrome, also known as benign form of Worth hyperostosis corticalis generalisata with torus platinus, autosomal dominant osteosclerosis, autosomal dominant endosteal hyperostosis or Worth disease, is a rare autosomal dominant congenital disorder that is caused by a mutation in the LRP5 gene. It is characterized by increased bone density and benign bony structures on the palate.".
- Worth_syndrome label "Worth syndrome".
- Worth_syndrome sameAs Q8037184.
- Worth_syndrome sameAs m.05p7hlm.
- Worth_syndrome sameAs Q8037184.
- Worth_syndrome wasDerivedFrom Worth_syndrome?oldid=679117928.
- Worth_syndrome depiction Autosomal_dominant_-_en.svg.
- Worth_syndrome isPrimaryTopicOf Worth_syndrome.
- Worth_syndrome name "Worth syndrome".