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- Sensenbrenner_syndrome abstract "Sensenbrenner syndrome (OMIM #218330) is a rare (less than 20 cases reported by 2010) multisystem disease first described in 1975. It is inherited in an autosomal recessive fashion, and a number of genes appear to be responsible. Three genes responsible have been identified: intraflagellar transport (IFT)122 (WDR10), IFT43 - a subunit of the IFT complex A machinery of primary cilia, and WDR35 (IFT121: TULP4)It is also known as Sensenbrenner–Dorst–Owens syndrome, Levin Syndrome I and cranioectodermal dysplasia (CED)".
- Sensenbrenner_syndrome wikiPageID "31121758".
- Sensenbrenner_syndrome wikiPageLength "5727".
- Sensenbrenner_syndrome wikiPageOutDegree "19".
- Sensenbrenner_syndrome wikiPageRevisionID "553737809".
- Sensenbrenner_syndrome wikiPageWikiLink Atomic_mass_unit.
- Sensenbrenner_syndrome wikiPageWikiLink Brachydactyly.
- Sensenbrenner_syndrome wikiPageWikiLink Category:Syndromes.
- Sensenbrenner_syndrome wikiPageWikiLink Chromosome_14.
- Sensenbrenner_syndrome wikiPageWikiLink Chromosome_14_(human).
- Sensenbrenner_syndrome wikiPageWikiLink Chromosome_2.
- Sensenbrenner_syndrome wikiPageWikiLink Chromosome_2_(human).
- Sensenbrenner_syndrome wikiPageWikiLink Chromosome_3.
- Sensenbrenner_syndrome wikiPageWikiLink Chromosome_3_(human).
- Sensenbrenner_syndrome wikiPageWikiLink Cilium.
- Sensenbrenner_syndrome wikiPageWikiLink Corpus_callosum.
- Sensenbrenner_syndrome wikiPageWikiLink Dalton_(unit).
- Sensenbrenner_syndrome wikiPageWikiLink Dolichocephaly.
- Sensenbrenner_syndrome wikiPageWikiLink Dynein.
- Sensenbrenner_syndrome wikiPageWikiLink Electroretinography.
- Sensenbrenner_syndrome wikiPageWikiLink Hypodontia.
- Sensenbrenner_syndrome wikiPageWikiLink Hypohydrosis.
- Sensenbrenner_syndrome wikiPageWikiLink Intraflagellar_transport.
- Sensenbrenner_syndrome wikiPageWikiLink Kinesin.
- Sensenbrenner_syndrome wikiPageWikiLink Microcephaly.
- Sensenbrenner_syndrome wikiPageWikiLink Microdontia.
- Sensenbrenner_syndrome wikiPageWikiLink Rhizomelic_dwarfism.
- Sensenbrenner_syndrome wikiPageWikiLink Sonic_hedgehog.
- Sensenbrenner_syndrome wikiPageWikiLinkText "Sensenbrenner syndrome".
- Sensenbrenner_syndrome hasPhotoCollection Sensenbrenner_syndrome.
- Sensenbrenner_syndrome wikiPageUsesTemplate Template:Reflist.
- Sensenbrenner_syndrome subject Category:Syndromes.
- Sensenbrenner_syndrome hypernym Disease.
- Sensenbrenner_syndrome type Disease.
- Sensenbrenner_syndrome type Syndrome.
- Sensenbrenner_syndrome comment "Sensenbrenner syndrome (OMIM #218330) is a rare (less than 20 cases reported by 2010) multisystem disease first described in 1975. It is inherited in an autosomal recessive fashion, and a number of genes appear to be responsible.".
- Sensenbrenner_syndrome label "Sensenbrenner syndrome".
- Sensenbrenner_syndrome sameAs m.0gh8svj.
- Sensenbrenner_syndrome sameAs Q7451019.
- Sensenbrenner_syndrome sameAs Q7451019.
- Sensenbrenner_syndrome wasDerivedFrom Sensenbrenner_syndrome?oldid=553737809.
- Sensenbrenner_syndrome isPrimaryTopicOf Sensenbrenner_syndrome.