Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/FG_syndrome> ?p ?o }
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- FG_syndrome abstract "FG syndrome (FGS; also known as Opitz–Kaveggia syndrome) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. First reported by Opitz and Kaveggia in 1974, its major clinical features include intellectual disability, hyperactivity, hypotonia (low muscle tone), and a characteristic facial appearance including macrocephaly (an abnormally large head).".
- FG_syndrome wikiPageID "20545450".
- FG_syndrome wikiPageLength "3452".
- FG_syndrome wikiPageOutDegree "21".
- FG_syndrome wikiPageRevisionID "667966651".
- FG_syndrome wikiPageWikiLink Attention_deficit_hyperactivity_disorder.
- FG_syndrome wikiPageWikiLink Autism.
- FG_syndrome wikiPageWikiLink CASK.
- FG_syndrome wikiPageWikiLink Category:Syndromes.
- FG_syndrome wikiPageWikiLink Category:X-linked_recessive_disorders.
- FG_syndrome wikiPageWikiLink Corpus_callosum.
- FG_syndrome wikiPageWikiLink Dustin_Hoffman.
- FG_syndrome wikiPageWikiLink FLNA.
- FG_syndrome wikiPageWikiLink Hypotonia.
- FG_syndrome wikiPageWikiLink Imperforate_anus.
- FG_syndrome wikiPageWikiLink Intellectual_disability.
- FG_syndrome wikiPageWikiLink Kim_Peek.
- FG_syndrome wikiPageWikiLink Lujan–Fryns_syndrome.
- FG_syndrome wikiPageWikiLink MED12.
- FG_syndrome wikiPageWikiLink Macrocephaly.
- FG_syndrome wikiPageWikiLink Online_Mendelian_Inheritance_in_Man.
- FG_syndrome wikiPageWikiLink Rain_Man.
- FG_syndrome wikiPageWikiLink X_chromosome.
- FG_syndrome wikiPageWikiLink File:Kim_Peek,_diagnosed_with_Savant_syndrome.jpg.
- FG_syndrome wikiPageWikiLinkText "FG syndrome".
- FG_syndrome wikiPageWikiLinkText "Opitz-Kaveggia (FGS1) syndrome".
- FG_syndrome wikiPageWikiLinkText "Opitz-Kaveggia syndrome".
- FG_syndrome diseasesdb "32162".
- FG_syndrome genereviewsname "MED12-related disorders".
- FG_syndrome genereviewsnbk "NBK1676".
- FG_syndrome name "FG syndrome".
- FG_syndrome omim "305450".
- FG_syndrome wikiPageUsesTemplate Template:Cytoskeletal_defects.
- FG_syndrome wikiPageUsesTemplate Template:Infobox_Disease.
- FG_syndrome wikiPageUsesTemplate Template:OMIM2.
- FG_syndrome wikiPageUsesTemplate Template:Reflist.
- FG_syndrome wikiPageUsesTemplate Template:X-linked_disorders.
- FG_syndrome subject Category:Syndromes.
- FG_syndrome subject Category:X-linked_recessive_disorders.
- FG_syndrome hypernym Syndrome.
- FG_syndrome type Disease.
- FG_syndrome type Disorder.
- FG_syndrome type Redirect.
- FG_syndrome type Syndrome.
- FG_syndrome comment "FG syndrome (FGS; also known as Opitz–Kaveggia syndrome) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. First reported by Opitz and Kaveggia in 1974, its major clinical features include intellectual disability, hyperactivity, hypotonia (low muscle tone), and a characteristic facial appearance including macrocephaly (an abnormally large head).".
- FG_syndrome label "FG syndrome".
- FG_syndrome sameAs Q530142.
- FG_syndrome sameAs FG-Syndrom.
- FG_syndrome sameAs Síndrome_FG.
- FG_syndrome sameAs Syndrome_FG.
- FG_syndrome sameAs Zespół_Opitza-Kaveggii.
- FG_syndrome sameAs m.051whx6.
- FG_syndrome sameAs Q530142.
- FG_syndrome wasDerivedFrom FG_syndrome?oldid=667966651.
- FG_syndrome isPrimaryTopicOf FG_syndrome.