Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Catel–Manzke_syndrome> ?p ?o }
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- Catel–Manzke_syndrome abstract "Catel–Manzke syndrome is a rare genetic disorder characterized by distinctive abnormalities of the index fingers; the classic features of Pierre Robin syndrome; occasionally with additional physical findings. Pierre Robin syndrome refers to a sequence of abnormalities that may occur as a distinct syndrome or as part of another underlying disorder. Pierre Robin syndrome is characterized by an unusually small jaw (Micrognathia), downward displacement or retraction of the tongue (Glossoptosis), and incomplete closure of the roof of the mouth (Cleft palate). It is also linked to Hyper Mobility Syndrome.".
- Catel–Manzke_syndrome wikiPageID "6013274".
- Catel–Manzke_syndrome wikiPageLength "2494".
- Catel–Manzke_syndrome wikiPageOutDegree "23".
- Catel–Manzke_syndrome wikiPageRevisionID "660827891".
- Catel–Manzke_syndrome wikiPageWikiLink Bone.
- Catel–Manzke_syndrome wikiPageWikiLink Category:Genetic_disorders_with_OMIM_but_no_gene.
- Catel–Manzke_syndrome wikiPageWikiLink Category:Skeletal_disorders.
- Catel–Manzke_syndrome wikiPageWikiLink Category:Syndromes.
- Catel–Manzke_syndrome wikiPageWikiLink Cleft_lip_and_palate.
- Catel–Manzke_syndrome wikiPageWikiLink Cleft_palate.
- Catel–Manzke_syndrome wikiPageWikiLink Clinodactyly.
- Catel–Manzke_syndrome wikiPageWikiLink Dominance_(genetics).
- Catel–Manzke_syndrome wikiPageWikiLink Ear_infection.
- Catel–Manzke_syndrome wikiPageWikiLink Genetic_disorder.
- Catel–Manzke_syndrome wikiPageWikiLink Glossoptosis.
- Catel–Manzke_syndrome wikiPageWikiLink Heart.
- Catel–Manzke_syndrome wikiPageWikiLink Hyperphalangy.
- Catel–Manzke_syndrome wikiPageWikiLink Jaw.
- Catel–Manzke_syndrome wikiPageWikiLink Metacarpal.
- Catel–Manzke_syndrome wikiPageWikiLink Metacarpus.
- Catel–Manzke_syndrome wikiPageWikiLink Micrognathia.
- Catel–Manzke_syndrome wikiPageWikiLink Micrognathism.
- Catel–Manzke_syndrome wikiPageWikiLink Otitis.
- Catel–Manzke_syndrome wikiPageWikiLink Otitis_media.
- Catel–Manzke_syndrome wikiPageWikiLink Phalanx_bone.
- Catel–Manzke_syndrome wikiPageWikiLink Pierre_Robin_syndrome.
- Catel–Manzke_syndrome wikiPageWikiLink Proximal_phalanx.
- Catel–Manzke_syndrome wikiPageWikiLink Recessive_gene.
- Catel–Manzke_syndrome wikiPageWikiLink Sex_linkage.
- Catel–Manzke_syndrome wikiPageWikiLink Tongue.
- Catel–Manzke_syndrome wikiPageWikiLinkText "Catel–Manzke syndrome".
- Catel–Manzke_syndrome diseasesdb "33832".
- Catel–Manzke_syndrome hasPhotoCollection Catel–Manzke_syndrome.
- Catel–Manzke_syndrome name "Catel–Manzke syndrome".
- Catel–Manzke_syndrome omim "302380".
- Catel–Manzke_syndrome wikiPageUsesTemplate Template:Infobox_Disease.
- Catel–Manzke_syndrome wikiPageUsesTemplate Template:Phakomatoses_and_other_congenital_malformations_not_elsewhere_classified.
- Catel–Manzke_syndrome wikiPageUsesTemplate Template:Refimprove.
- Catel–Manzke_syndrome wikiPageUsesTemplate Template:Reflist.
- Catel–Manzke_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Catel–Manzke_syndrome subject Category:Skeletal_disorders.
- Catel–Manzke_syndrome subject Category:Syndromes.
- Catel–Manzke_syndrome comment "Catel–Manzke syndrome is a rare genetic disorder characterized by distinctive abnormalities of the index fingers; the classic features of Pierre Robin syndrome; occasionally with additional physical findings. Pierre Robin syndrome refers to a sequence of abnormalities that may occur as a distinct syndrome or as part of another underlying disorder.".
- Catel–Manzke_syndrome label "Catel–Manzke syndrome".
- Catel–Manzke_syndrome sameAs Zespół_Catela-Manzkego.
- Catel–Manzke_syndrome sameAs m.0fklf5.
- Catel–Manzke_syndrome sameAs Q5051865.
- Catel–Manzke_syndrome sameAs Q5051865.
- Catel–Manzke_syndrome wasDerivedFrom Catel–Manzke_syndrome?oldid=660827891.
- Catel–Manzke_syndrome isPrimaryTopicOf Catel–Manzke_syndrome.