Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Rudiger_syndrome> ?p ?o }
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- Rudiger_syndrome abstract "Rudiger syndrome is a congenital disorder characterized by the association of severe growth retardation with abnormalities of the extremities, urogenital abnormalities and facial abnormalities. It has been described in a family where an affected brother and sister died as infants. Both autosomal recessive and autosomal dominant inheritance have been suggested with the disorder.The features ectrodactyly, ectodermal dysplasia and cleft palate have been described with Rudiger syndrome, giving it the rarely used designation \"EEC syndrome\". However, this is not to be confused with the formal EEC syndrome associated with chromosome 7.It was characterized in 1971.".
- Rudiger_syndrome omim "268650".
- Rudiger_syndrome wikiPageID "25333765".
- Rudiger_syndrome wikiPageLength "2468".
- Rudiger_syndrome wikiPageOutDegree "13".
- Rudiger_syndrome wikiPageRevisionID "705843651".
- Rudiger_syndrome wikiPageWikiLink Autosome.
- Rudiger_syndrome wikiPageWikiLink Category:Congenital_disorders.
- Rudiger_syndrome wikiPageWikiLink Category:Genetic_disorders_with_OMIM_but_no_gene.
- Rudiger_syndrome wikiPageWikiLink Category:Rare_diseases.
- Rudiger_syndrome wikiPageWikiLink Category:Syndromes.
- Rudiger_syndrome wikiPageWikiLink Chromosome_7_(human).
- Rudiger_syndrome wikiPageWikiLink Cleft_lip_and_palate.
- Rudiger_syndrome wikiPageWikiLink Congenital_disorder.
- Rudiger_syndrome wikiPageWikiLink Dominance_(genetics).
- Rudiger_syndrome wikiPageWikiLink Ectodermal_dysplasia.
- Rudiger_syndrome wikiPageWikiLink Ectrodactyly.
- Rudiger_syndrome wikiPageWikiLink Ectrodactyly–ectodermal_dysplasia–cleft_syndrome.
- Rudiger_syndrome wikiPageWikiLinkText "Rudiger syndrome".
- Rudiger_syndrome name "Rudiger syndrome".
- Rudiger_syndrome omim "268650".
- Rudiger_syndrome wikiPageUsesTemplate Template:Genetic-disorder-stub.
- Rudiger_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Rudiger_syndrome wikiPageUsesTemplate Template:Reflist.
- Rudiger_syndrome subject Category:Congenital_disorders.
- Rudiger_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Rudiger_syndrome subject Category:Rare_diseases.
- Rudiger_syndrome subject Category:Syndromes.
- Rudiger_syndrome hypernym Disorder.
- Rudiger_syndrome type Disease.
- Rudiger_syndrome type Disorder.
- Rudiger_syndrome type Pediatric.
- Rudiger_syndrome type Syndrome.
- Rudiger_syndrome type Thing.
- Rudiger_syndrome type Q12136.
- Rudiger_syndrome comment "Rudiger syndrome is a congenital disorder characterized by the association of severe growth retardation with abnormalities of the extremities, urogenital abnormalities and facial abnormalities. It has been described in a family where an affected brother and sister died as infants.".
- Rudiger_syndrome label "Rudiger syndrome".
- Rudiger_syndrome sameAs Q7376987.
- Rudiger_syndrome sameAs متلازمة_روديجر.
- Rudiger_syndrome sameAs Rudigerin_oireyhtymä.
- Rudiger_syndrome sameAs m.09gh642.
- Rudiger_syndrome sameAs Q7376987.
- Rudiger_syndrome wasDerivedFrom Rudiger_syndrome?oldid=705843651.
- Rudiger_syndrome isPrimaryTopicOf Rudiger_syndrome.
- Rudiger_syndrome name "Rudiger syndrome".