Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Pitt–Hopkins_syndrome> ?p ?o. }
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- Pitt–Hopkins_syndrome abstract "Pitt–Hopkins syndrome is a genetic disorder characterized by developmental delay, a wide mouth, distinctive facial features, and intermittent hyperventilation followed by apnea. It is associated with an abnormality within chromosome 18: specifically, it is caused by an insufficient expression of the TCF4 gene.".
- Pitt–Hopkins_syndrome wikiPageID "25342738".
- Pitt–Hopkins_syndrome wikiPageRevisionID "600801976".
- Pitt–Hopkins_syndrome name "Pitt–Hopkins syndrome".
- Pitt–Hopkins_syndrome omim "610954".
- Pitt–Hopkins_syndrome subject Category:Syndromes.
- Pitt–Hopkins_syndrome subject Category:Transcription_factor_deficiencies.
- Pitt–Hopkins_syndrome type Disease.
- Pitt–Hopkins_syndrome type Situation.
- Pitt–Hopkins_syndrome comment "Pitt–Hopkins syndrome is a genetic disorder characterized by developmental delay, a wide mouth, distinctive facial features, and intermittent hyperventilation followed by apnea. It is associated with an abnormality within chromosome 18: specifically, it is caused by an insufficient expression of the TCF4 gene.".
- Pitt–Hopkins_syndrome label "Pitt-Hopkins-Syndrom".
- Pitt–Hopkins_syndrome label "Pitt–Hopkins syndrome".
- Pitt–Hopkins_syndrome label "Синдром Питта — Хопкинса".
- Pitt–Hopkins_syndrome sameAs Pitt%E2%80%93Hopkins_syndrome.
- Pitt–Hopkins_syndrome sameAs Pitt-Hopkins-Syndrom.
- Pitt–Hopkins_syndrome sameAs Q1164401.
- Pitt–Hopkins_syndrome sameAs Q1164401.
- Pitt–Hopkins_syndrome wasDerivedFrom Pitt–Hopkins_syndrome?oldid=600801976.