Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Pitt–Hopkins_syndrome> ?p ?o }
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- Pitt–Hopkins_syndrome abstract "Pitt–Hopkins syndrome is a rare 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 omim "610954".
- Pitt–Hopkins_syndrome wikiPageID "25342738".
- Pitt–Hopkins_syndrome wikiPageLength "5650".
- Pitt–Hopkins_syndrome wikiPageOutDegree "42".
- Pitt–Hopkins_syndrome wikiPageRevisionID "681782625".
- Pitt–Hopkins_syndrome wikiPageWikiLink Aerophagia.
- Pitt–Hopkins_syndrome wikiPageWikiLink Angelman_syndrome.
- Pitt–Hopkins_syndrome wikiPageWikiLink Apnea.
- Pitt–Hopkins_syndrome wikiPageWikiLink CNTN1.
- Pitt–Hopkins_syndrome wikiPageWikiLink CNTNAP2.
- Pitt–Hopkins_syndrome wikiPageWikiLink Category:Syndromes.
- Pitt–Hopkins_syndrome wikiPageWikiLink Category:Transcription_factor_deficiencies.
- Pitt–Hopkins_syndrome wikiPageWikiLink Caudate_nucleus.
- Pitt–Hopkins_syndrome wikiPageWikiLink Chromosome_18.
- Pitt–Hopkins_syndrome wikiPageWikiLink Chromosome_18_(human).
- Pitt–Hopkins_syndrome wikiPageWikiLink Chromosome_2.
- Pitt–Hopkins_syndrome wikiPageWikiLink Chromosome_2_(human).
- Pitt–Hopkins_syndrome wikiPageWikiLink Chromosome_7.
- Pitt–Hopkins_syndrome wikiPageWikiLink Chromosome_7_(human).
- Pitt–Hopkins_syndrome wikiPageWikiLink Contactin.
- Pitt–Hopkins_syndrome wikiPageWikiLink Corpus_callosum.
- Pitt–Hopkins_syndrome wikiPageWikiLink Cryptorchidism.
- Pitt–Hopkins_syndrome wikiPageWikiLink Cupids_bow.
- Pitt–Hopkins_syndrome wikiPageWikiLink Cutaneous_condition.
- Pitt–Hopkins_syndrome wikiPageWikiLink Cyanosis.
- Pitt–Hopkins_syndrome wikiPageWikiLink Distal_18q-.
- Pitt–Hopkins_syndrome wikiPageWikiLink Electroencephalogram.
- Pitt–Hopkins_syndrome wikiPageWikiLink Electroencephalography.
- Pitt–Hopkins_syndrome wikiPageWikiLink Epileptic_seizure.
- Pitt–Hopkins_syndrome wikiPageWikiLink Facial.
- Pitt–Hopkins_syndrome wikiPageWikiLink Feral_child.
- Pitt–Hopkins_syndrome wikiPageWikiLink File:Peter_the_Wild_Boy.jpg.
- Pitt–Hopkins_syndrome wikiPageWikiLink Hyperventilation.
- Pitt–Hopkins_syndrome wikiPageWikiLink Hypotonia.
- Pitt–Hopkins_syndrome wikiPageWikiLink IgM.
- Pitt–Hopkins_syndrome wikiPageWikiLink Immunoglobulin_M.
- Pitt–Hopkins_syndrome wikiPageWikiLink Macule.
- Pitt–Hopkins_syndrome wikiPageWikiLink Microcephaly.
- Pitt–Hopkins_syndrome wikiPageWikiLink Mouth.
- Pitt–Hopkins_syndrome wikiPageWikiLink Mowat–Wilson_syndrome.
- Pitt–Hopkins_syndrome wikiPageWikiLink Myopia.
- Pitt–Hopkins_syndrome wikiPageWikiLink NRXN1.
- Pitt–Hopkins_syndrome wikiPageWikiLink Neurexin.
- Pitt–Hopkins_syndrome wikiPageWikiLink Peter_the_Wild_Boy.
- Pitt–Hopkins_syndrome wikiPageWikiLink Rett_syndrome.
- Pitt–Hopkins_syndrome wikiPageWikiLink Rostrum_of_corpus_callosum.
- Pitt–Hopkins_syndrome wikiPageWikiLink Seizure.
- Pitt–Hopkins_syndrome wikiPageWikiLink Specific_developmental_disorder.
- Pitt–Hopkins_syndrome wikiPageWikiLink Splenium.
- Pitt–Hopkins_syndrome wikiPageWikiLink Strabismus.
- Pitt–Hopkins_syndrome wikiPageWikiLink TCF4.
- Pitt–Hopkins_syndrome wikiPageWikiLinkText "Pitt–Hopkins syndrome".
- Pitt–Hopkins_syndrome hasPhotoCollection Pitt–Hopkins_syndrome.
- Pitt–Hopkins_syndrome name "Pitt–Hopkins syndrome".
- Pitt–Hopkins_syndrome omim "610954".
- Pitt–Hopkins_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Pitt–Hopkins_syndrome wikiPageUsesTemplate coregulator_deficiencies.
- Pitt–Hopkins_syndrome subject Category:Syndromes.
- Pitt–Hopkins_syndrome subject Category:Transcription_factor_deficiencies.
- Pitt–Hopkins_syndrome type Disease.
- Pitt–Hopkins_syndrome type Thing.
- Pitt–Hopkins_syndrome type Q12136.
- Pitt–Hopkins_syndrome comment "Pitt–Hopkins syndrome is a rare 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 syndrome".
- Pitt–Hopkins_syndrome sameAs Сіндром_Піта-Хопкінса.
- Pitt–Hopkins_syndrome sameAs Pitt-Hopkins-Syndrom.
- Pitt–Hopkins_syndrome sameAs Siondróm_Pitt-Hopkins.
- Pitt–Hopkins_syndrome sameAs Sindrome_di_Pitt-Hopkins.
- Pitt–Hopkins_syndrome sameAs m.09glx9m.
- Pitt–Hopkins_syndrome sameAs Синдром_Питта_—_Хопкинса.
- Pitt–Hopkins_syndrome sameAs Q1164401.
- Pitt–Hopkins_syndrome sameAs Q1164401.
- Pitt–Hopkins_syndrome wasDerivedFrom Pitt–Hopkins_syndrome?oldid=681782625.
- Pitt–Hopkins_syndrome isPrimaryTopicOf Pitt–Hopkins_syndrome.
- Pitt–Hopkins_syndrome name "Pitt–Hopkins syndrome".