Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/3-M_syndrome> ?p ?o }
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- 3-M_syndrome abstract "3-M syndrome (alternative names: dolichospondylic dysplasia, gloomy face syndrome and le Merrer syndrome) is a rare hereditary growth retardation syndrome. The name 3-M originates from the initials of the three authors Miller, McKusick and Malvaux who first reported the syndrome in literature. Major symptoms of 3M syndrome are dwarfism, facial dysmorphia and skeletal abnormalities. No signs of mental retardation are reported. 3-M syndrome is thought to be inherited as an autosomal recessive genetic trait.".
- 3-M_syndrome icd10 "Q87.1".
- 3-M_syndrome icd9 "xxx".
- 3-M_syndrome omim "273750".
- 3-M_syndrome wikiPageExternalLink NBK1481.
- 3-M_syndrome wikiPageExternalLink 273750,609577,610991,612921,273750,609577,610991,612921.
- 3-M_syndrome wikiPageID "17533758".
- 3-M_syndrome wikiPageLength "7824".
- 3-M_syndrome wikiPageOutDegree "8".
- 3-M_syndrome wikiPageRevisionID "658972080".
- 3-M_syndrome wikiPageWikiLink CUL7.
- 3-M_syndrome wikiPageWikiLink Category:Disorders_of_synthesis_of_DNA,_RNA,_and_proteins.
- 3-M_syndrome wikiPageWikiLink Category:Syndromes.
- 3-M_syndrome wikiPageWikiLink DNA_bank.
- 3-M_syndrome wikiPageWikiLink Dominance_(genetics).
- 3-M_syndrome wikiPageWikiLink Dwarfism.
- 3-M_syndrome wikiPageWikiLink Intellectual_disability.
- 3-M_syndrome wikiPageWikiLink Ubiquitin.
- 3-M_syndrome wikiPageWikiLinkText "3-M syndrome".
- 3-M_syndrome diseasesdb "33510".
- 3-M_syndrome genereviewsname "3".
- 3-M_syndrome genereviewsnbk "NBK1481".
- 3-M_syndrome icd "Q87.1".
- 3-M_syndrome icd "xxx".
- 3-M_syndrome name "3".
- 3-M_syndrome omim "273750".
- 3-M_syndrome wikiPageUsesTemplate Template:Disorders_of_translation_and_posttranslational_modification.
- 3-M_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- 3-M_syndrome wikiPageUsesTemplate Template:OMIM2.
- 3-M_syndrome wikiPageUsesTemplate Template:Reflist.
- 3-M_syndrome subject Category:Disorders_of_synthesis_of_DNA,_RNA,_and_proteins.
- 3-M_syndrome subject Category:Syndromes.
- 3-M_syndrome hypernym Syndrome.
- 3-M_syndrome type Disease.
- 3-M_syndrome type Disorder.
- 3-M_syndrome type Redirect.
- 3-M_syndrome type Syndrome.
- 3-M_syndrome type Thing.
- 3-M_syndrome type Q12136.
- 3-M_syndrome comment "3-M syndrome (alternative names: dolichospondylic dysplasia, gloomy face syndrome and le Merrer syndrome) is a rare hereditary growth retardation syndrome. The name 3-M originates from the initials of the three authors Miller, McKusick and Malvaux who first reported the syndrome in literature. Major symptoms of 3M syndrome are dwarfism, facial dysmorphia and skeletal abnormalities. No signs of mental retardation are reported.".
- 3-M_syndrome label "3-M syndrome".
- 3-M_syndrome sameAs Q3335660.
- 3-M_syndrome sameAs متلازمة_M-3.
- 3-M_syndrome sameAs 3M-Syndrom.
- 3-M_syndrome sameAs Síndrome_3-M.
- 3-M_syndrome sameAs Nanisme_3M.
- 3-M_syndrome sameAs Zespół_%22trzech_M%22.
- 3-M_syndrome sameAs m.02qt39n.
- 3-M_syndrome sameAs Q3335660.
- 3-M_syndrome wasDerivedFrom 3-M_syndrome?oldid=658972080.
- 3-M_syndrome isPrimaryTopicOf 3-M_syndrome.
- 3-M_syndrome name "3-M syndrome".