Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Fitzsimmons–Guilbert_syndrome> ?p ?o }
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- Fitzsimmons–Guilbert_syndrome abstract "Fitzsimmons–Guilbert syndrome is an extremely rare genetic disease characterized by a slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit.".
- Fitzsimmons–Guilbert_syndrome omim "270710".
- Fitzsimmons–Guilbert_syndrome wikiPageID "9978628".
- Fitzsimmons–Guilbert_syndrome wikiPageLength "3308".
- Fitzsimmons–Guilbert_syndrome wikiPageOutDegree "10".
- Fitzsimmons–Guilbert_syndrome wikiPageRevisionID "551301503".
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Brachydactyly.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Category:Genetic_disorders_with_OMIM_but_no_gene.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Category:Rare_diseases.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Dysarthria.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Epiphyses.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Epiphysis.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Human_sternum.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Metaphyseal.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Metaphysis.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Paraplegia.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Pectus_carinatum.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Phalanx_bone.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Phalanx_bones.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLink Sternum.
- Fitzsimmons–Guilbert_syndrome wikiPageWikiLinkText "Fitzsimmons–Guilbert syndrome".
- Fitzsimmons–Guilbert_syndrome hasPhotoCollection Fitzsimmons–Guilbert_syndrome.
- Fitzsimmons–Guilbert_syndrome name "Fitzsimmons–Guilbert syndrome".
- Fitzsimmons–Guilbert_syndrome omim "270710".
- Fitzsimmons–Guilbert_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Fitzsimmons–Guilbert_syndrome wikiPageUsesTemplate Template:Orphan.
- Fitzsimmons–Guilbert_syndrome wikiPageUsesTemplate Template:Reflist.
- Fitzsimmons–Guilbert_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Fitzsimmons–Guilbert_syndrome subject Category:Rare_diseases.
- Fitzsimmons–Guilbert_syndrome type Disease.
- Fitzsimmons–Guilbert_syndrome type Thing.
- Fitzsimmons–Guilbert_syndrome type Q12136.
- Fitzsimmons–Guilbert_syndrome comment "Fitzsimmons–Guilbert syndrome is an extremely rare genetic disease characterized by a slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit.".
- Fitzsimmons–Guilbert_syndrome label "Fitzsimmons–Guilbert syndrome".
- Fitzsimmons–Guilbert_syndrome sameAs Fitzsimmons-Guilbert-Syndrom.
- Fitzsimmons–Guilbert_syndrome sameAs m.02pyrj5.
- Fitzsimmons–Guilbert_syndrome sameAs Q5455731.
- Fitzsimmons–Guilbert_syndrome sameAs Q5455731.
- Fitzsimmons–Guilbert_syndrome wasDerivedFrom Fitzsimmons–Guilbert_syndrome?oldid=551301503.
- Fitzsimmons–Guilbert_syndrome isPrimaryTopicOf Fitzsimmons–Guilbert_syndrome.
- Fitzsimmons–Guilbert_syndrome name "Fitzsimmons–Guilbert syndrome".