Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Muenke_syndrome> ?p ?o }
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- Muenke_syndrome abstract "Muenke syndrome, also known as FGFR3-related craniosynostosis, is a human specific condition characterized by the premature closure of certain bones of the skull during development, which affects the shape of the head and face. First described by Maximilian Muenke, the syndrome occurs in about 1 in 30,000 newborns. This condition accounts for an estimated 8 percent of all cases of craniosynostosis.".
- Muenke_syndrome icd10 "Q75.0".
- Muenke_syndrome omim "602849".
- Muenke_syndrome wikiPageExternalLink condition=muenkesyndrome.
- Muenke_syndrome wikiPageExternalLink Muenke.htm.
- Muenke_syndrome wikiPageExternalLink NBK1415.
- Muenke_syndrome wikiPageID "9350855".
- Muenke_syndrome wikiPageLength "7922".
- Muenke_syndrome wikiPageOutDegree "19".
- Muenke_syndrome wikiPageRevisionID "654743384".
- Muenke_syndrome wikiPageWikiLink Autosomal_dominant.
- Muenke_syndrome wikiPageWikiLink Bone.
- Muenke_syndrome wikiPageWikiLink Category:Cell_surface_receptor_deficiencies.
- Muenke_syndrome wikiPageWikiLink Category:Congenital_disorders.
- Muenke_syndrome wikiPageWikiLink Category:Neurological_disorders.
- Muenke_syndrome wikiPageWikiLink Child_development.
- Muenke_syndrome wikiPageWikiLink Coronal_suture.
- Muenke_syndrome wikiPageWikiLink Craniosynostosis.
- Muenke_syndrome wikiPageWikiLink Dominance_(genetics).
- Muenke_syndrome wikiPageWikiLink FGFR3.
- Muenke_syndrome wikiPageWikiLink Face.
- Muenke_syndrome wikiPageWikiLink Fibroblast_growth_factor_receptor_3.
- Muenke_syndrome wikiPageWikiLink Gene_mutation.
- Muenke_syndrome wikiPageWikiLink Head.
- Muenke_syndrome wikiPageWikiLink Hearing_loss.
- Muenke_syndrome wikiPageWikiLink Human_skull.
- Muenke_syndrome wikiPageWikiLink Infant.
- Muenke_syndrome wikiPageWikiLink Learning_disabilities.
- Muenke_syndrome wikiPageWikiLink Learning_disability.
- Muenke_syndrome wikiPageWikiLink Macrocephaly.
- Muenke_syndrome wikiPageWikiLink Mutation.
- Muenke_syndrome wikiPageWikiLink Newborn.
- Muenke_syndrome wikiPageWikiLink File:Autosomal_Dominant_Pedigree_Chart.svg.
- Muenke_syndrome wikiPageWikiLinkText "Muenke syndrome".
- Muenke_syndrome wikiPageWikiLinkText "Muenke".
- Muenke_syndrome diseasesdb "33585".
- Muenke_syndrome genereviewsname "Muenke Syndrome".
- Muenke_syndrome genereviewsnbk "NBK1415".
- Muenke_syndrome hasPhotoCollection Muenke_syndrome.
- Muenke_syndrome icd "Q75.0".
- Muenke_syndrome name "Muenke syndrome".
- Muenke_syndrome omim "602849".
- Muenke_syndrome wikiPageUsesTemplate Template:Cell_surface_receptor_deficiencies.
- Muenke_syndrome wikiPageUsesTemplate Template:Cite_journal.
- Muenke_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Muenke_syndrome wikiPageUsesTemplate Template:Reflist.
- Muenke_syndrome subject Category:Cell_surface_receptor_deficiencies.
- Muenke_syndrome subject Category:Congenital_disorders.
- Muenke_syndrome subject Category:Neurological_disorders.
- Muenke_syndrome hypernym Condition.
- Muenke_syndrome type Disease.
- Muenke_syndrome type Deficiency.
- Muenke_syndrome type Disorder.
- Muenke_syndrome type Pediatric.
- Muenke_syndrome type Thing.
- Muenke_syndrome type Q12136.
- Muenke_syndrome comment "Muenke syndrome, also known as FGFR3-related craniosynostosis, is a human specific condition characterized by the premature closure of certain bones of the skull during development, which affects the shape of the head and face. First described by Maximilian Muenke, the syndrome occurs in about 1 in 30,000 newborns. This condition accounts for an estimated 8 percent of all cases of craniosynostosis.".
- Muenke_syndrome label "Muenke syndrome".
- Muenke_syndrome sameAs Muenke-Syndrom.
- Muenke_syndrome sameAs Syndrome_de_Muenke.
- Muenke_syndrome sameAs m.0285k8y.
- Muenke_syndrome sameAs Q3508679.
- Muenke_syndrome sameAs Q3508679.
- Muenke_syndrome wasDerivedFrom Muenke_syndrome?oldid=654743384.
- Muenke_syndrome isPrimaryTopicOf Muenke_syndrome.
- Muenke_syndrome name "Muenke syndrome".