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- Peters-plus_syndrome abstract "Krause–van Schooneveld–Kivlin syndrome is a hereditary syndrome that mainly affects the eyes, growth and development of the individual. It is also known as Krause–Kivlin syndrome or Peters-plus syndrome.Features of this syndrome include Peters anomaly, leukoma (corneal opacity), central defect of Descemet's membrane, and shallow anterior chamber with synechiae between the iris and cornea. It is associated with short limb dwarfism and delayed mental development.Krause–van Schooneveld–Kivlin syndrome is listed as a \"rare disease\" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH), which means that the syndrome, or a subtype, affects fewer than 200,000 people in the United States.It is associated with the enzyme B3GALTL.It was characterized in 1984 by van Schooneveld.".
- Peters-plus_syndrome omim "261540".
- Peters-plus_syndrome wikiPageExternalLink br.fcgi?book=gene&part=peters-plus.
- Peters-plus_syndrome wikiPageExternalLink 261540,610308,261540,610308.
- Peters-plus_syndrome wikiPageID "10104641".
- Peters-plus_syndrome wikiPageLength "3006".
- Peters-plus_syndrome wikiPageOutDegree "15".
- Peters-plus_syndrome wikiPageRevisionID "679011677".
- Peters-plus_syndrome wikiPageWikiLink Anterior_segment_mesenchymal_dysgenesis.
- Peters-plus_syndrome wikiPageWikiLink B3GALTL.
- Peters-plus_syndrome wikiPageWikiLink Category:Rare_diseases.
- Peters-plus_syndrome wikiPageWikiLink Category:Syndromes.
- Peters-plus_syndrome wikiPageWikiLink Child_development.
- Peters-plus_syndrome wikiPageWikiLink Corneal_opacity.
- Peters-plus_syndrome wikiPageWikiLink Descemets_membrane.
- Peters-plus_syndrome wikiPageWikiLink Dwarfism.
- Peters-plus_syndrome wikiPageWikiLink EMedicine.
- Peters-plus_syndrome wikiPageWikiLink Heredity.
- Peters-plus_syndrome wikiPageWikiLink Human_development_(biology).
- Peters-plus_syndrome wikiPageWikiLink National_Institutes_of_Health.
- Peters-plus_syndrome wikiPageWikiLink Neural_development.
- Peters-plus_syndrome wikiPageWikiLink Syndrome.
- Peters-plus_syndrome wikiPageWikiLink Synechia_(eye).
- Peters-plus_syndrome wikiPageWikiLinkText "Peters-plus syndrome".
- Peters-plus_syndrome name "Peters-plus syndrome".
- Peters-plus_syndrome omim "261540".
- Peters-plus_syndrome wikiPageUsesTemplate Template:Disease-stub.
- Peters-plus_syndrome wikiPageUsesTemplate Template:EMedicine.
- Peters-plus_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Peters-plus_syndrome wikiPageUsesTemplate Template:Reflist.
- Peters-plus_syndrome subject Category:Rare_diseases.
- Peters-plus_syndrome subject Category:Syndromes.
- Peters-plus_syndrome hypernym Syndrome.
- Peters-plus_syndrome type Disease.
- Peters-plus_syndrome type Syndrome.
- Peters-plus_syndrome type Thing.
- Peters-plus_syndrome type Q12136.
- Peters-plus_syndrome comment "Krause–van Schooneveld–Kivlin syndrome is a hereditary syndrome that mainly affects the eyes, growth and development of the individual. It is also known as Krause–Kivlin syndrome or Peters-plus syndrome.Features of this syndrome include Peters anomaly, leukoma (corneal opacity), central defect of Descemet's membrane, and shallow anterior chamber with synechiae between the iris and cornea.".
- Peters-plus_syndrome label "Peters-plus syndrome".
- Peters-plus_syndrome sameAs Q7178104.
- Peters-plus_syndrome sameAs Zespół_Peters-plus.
- Peters-plus_syndrome sameAs m.02q1zhk.
- Peters-plus_syndrome sameAs Q7178104.
- Peters-plus_syndrome wasDerivedFrom Peters-plus_syndrome?oldid=679011677.
- Peters-plus_syndrome isPrimaryTopicOf Peters-plus_syndrome.
- Peters-plus_syndrome name "Peters-plus syndrome".