Matches in DBpedia 2014 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 linked to the X chromosome and causing physical anomalies and developmental delays. First reported by Opitz and Kaveggia in 1974, its major clinical features include retardation, hyperactivity, hypotonia (low muscle tone), and a characteristic facial appearance including macrocephaly (an abnormally large head).".
- FG_syndrome diseasesdb "32162".
- FG_syndrome omim "305450".
- FG_syndrome wikiPageID "20545450".
- FG_syndrome wikiPageRevisionID "595804317".
- FG_syndrome diseasesdb "32162".
- FG_syndrome genereviewsname "MED12-related disorders".
- FG_syndrome genereviewsnbk "NBK1676".
- FG_syndrome hasPhotoCollection FG_syndrome.
- FG_syndrome name "FG syndrome".
- FG_syndrome omim "305450".
- FG_syndrome subject Category:Syndromes.
- FG_syndrome subject Category:X-linked_recessive_disorders.
- FG_syndrome type Abstraction100002137.
- FG_syndrome type Attribute100024264.
- FG_syndrome type Cognition100023271.
- FG_syndrome type Complex105870365.
- FG_syndrome type Concept105835747.
- FG_syndrome type Condition113920835.
- FG_syndrome type Content105809192.
- FG_syndrome type Disease114070360.
- FG_syndrome type Disorder114052403.
- FG_syndrome type Idea105833840.
- FG_syndrome type IllHealth114052046.
- FG_syndrome type Illness114061805.
- FG_syndrome type PathologicalState114051917.
- FG_syndrome type PhysicalCondition114034177.
- FG_syndrome type PsychologicalFeature100023100.
- FG_syndrome type State100024720.
- FG_syndrome type Syndrome105870790.
- FG_syndrome type Syndromes.
- FG_syndrome type Whole105869584.
- FG_syndrome type X-linkedRecessiveDisorders.
- FG_syndrome type Disease.
- FG_syndrome type AilmentCondition.
- FG_syndrome type Situation.
- FG_syndrome comment "FG syndrome (FGS; also known as Opitz–Kaveggia syndrome) is a rare genetic syndrome linked to the X chromosome and causing physical anomalies and developmental delays. First reported by Opitz and Kaveggia in 1974, its major clinical features include retardation, hyperactivity, hypotonia (low muscle tone), and a characteristic facial appearance including macrocephaly (an abnormally large head).".
- FG_syndrome label "FG syndrome".
- FG_syndrome label "FG-Syndrom".
- FG_syndrome label "Syndrome FG".
- FG_syndrome label "Síndrome FG".
- FG_syndrome label "Zespół Opitza-Kaveggii".
- 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 sameAs Q530142.
- FG_syndrome sameAs FG_syndrome.
- FG_syndrome wasDerivedFrom FG_syndrome?oldid=595804317.
- FG_syndrome isPrimaryTopicOf FG_syndrome.
- FG_syndrome name "FG syndrome".