Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/18p-> ?p ?o }
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- 18p- abstract "18p- is a genetic condition caused by a deletion of all or part of the short arm (the p arm) of chromosome 18. It occurs in about 1 of every 40,000 births.".
- 18p- omim "146390".
- 18p- wikiPageExternalLink CDO.
- 18p- wikiPageExternalLink www.chromosome18.org.
- 18p- wikiPageExternalLink www.chromosome18eur.org.
- 18p- wikiPageExternalLink chromosome18.
- 18p- wikiPageExternalLink home.asp.
- 18p- wikiPageID "18832531".
- 18p- wikiPageLength "7070".
- 18p- wikiPageOutDegree "61".
- 18p- wikiPageRevisionID "619074161".
- 18p- wikiPageWikiLink Amniocentesis.
- 18p- wikiPageWikiLink Anxiety_disorder.
- 18p- wikiPageWikiLink Astigmatism.
- 18p- wikiPageWikiLink Category:Autosomal_monosomies_and_deletions.
- 18p- wikiPageWikiLink Centromere.
- 18p- wikiPageWikiLink Chorionic_villus_sampling.
- 18p- wikiPageWikiLink Club_foot.
- 18p- wikiPageWikiLink Coarctation_of_the_aorta.
- 18p- wikiPageWikiLink Cognition.
- 18p- wikiPageWikiLink Communication_disorder.
- 18p- wikiPageWikiLink Conductive_hearing_loss.
- 18p- wikiPageWikiLink Congenital_disorder.
- 18p- wikiPageWikiLink Congenital_heart_defect.
- 18p- wikiPageWikiLink Constipation.
- 18p- wikiPageWikiLink Corpus_callosum.
- 18p- wikiPageWikiLink Cryptorchidism.
- 18p- wikiPageWikiLink Cubitus_valgus.
- 18p- wikiPageWikiLink Developmental_coordination_disorder.
- 18p- wikiPageWikiLink Dextrocardia.
- 18p- wikiPageWikiLink Dystonia.
- 18p- wikiPageWikiLink Epicanthic_fold.
- 18p- wikiPageWikiLink Epileptic_seizure.
- 18p- wikiPageWikiLink Flat_feet.
- 18p- wikiPageWikiLink Genotyping.
- 18p- wikiPageWikiLink Genu_valgum.
- 18p- wikiPageWikiLink Growth_hormone_deficiency.
- 18p- wikiPageWikiLink Hernia.
- 18p- wikiPageWikiLink Hip_dysplasia.
- 18p- wikiPageWikiLink Holoprosencephaly.
- 18p- wikiPageWikiLink Hyperopia.
- 18p- wikiPageWikiLink Hypopituitarism.
- 18p- wikiPageWikiLink Hypothyroidism.
- 18p- wikiPageWikiLink Hypotonia.
- 18p- wikiPageWikiLink Intestinal_malrotation.
- 18p- wikiPageWikiLink Karyotype.
- 18p- wikiPageWikiLink Kyphosis.
- 18p- wikiPageWikiLink Locus_(genetics).
- 18p- wikiPageWikiLink Microarray.
- 18p- wikiPageWikiLink Mutation.
- 18p- wikiPageWikiLink Myopia.
- 18p- wikiPageWikiLink Nystagmus.
- 18p- wikiPageWikiLink Olfactory_bulb.
- 18p- wikiPageWikiLink Olfactory_tract.
- 18p- wikiPageWikiLink Otitis.
- 18p- wikiPageWikiLink Otitis_media.
- 18p- wikiPageWikiLink Pectus.
- 18p- wikiPageWikiLink Penetrance.
- 18p- wikiPageWikiLink Philtrum.
- 18p- wikiPageWikiLink Prenatal_diagnosis.
- 18p- wikiPageWikiLink Ptosis_(eyelid).
- 18p- wikiPageWikiLink Refractive_error.
- 18p- wikiPageWikiLink Scoliosis.
- 18p- wikiPageWikiLink Specific_developmental_disorder.
- 18p- wikiPageWikiLink Spina_bifida.
- 18p- wikiPageWikiLink Stereotypic_movement_disorder.
- 18p- wikiPageWikiLink Strabismus.
- 18p- wikiPageWikiLink Tethered_spinal_cord_syndrome.
- 18p- wikiPageWikiLink Tetralogy_of_Fallot.
- 18p- wikiPageWikiLink Tympanostomy_tube.
- 18p- wikiPageWikiLink File:FISH18.jpg.
- 18p- wikiPageWikiLinkText "18p-".
- 18p- name "18".
- 18p- omim "146390".
- 18p- wikiPageUsesTemplate Template:Infobox_disease.
- 18p- subject Category:Autosomal_monosomies_and_deletions.
- 18p- hypernym Condition.
- 18p- type Disease.
- 18p- type Thing.
- 18p- type Q12136.
- 18p- comment "18p- is a genetic condition caused by a deletion of all or part of the short arm (the p arm) of chromosome 18. It occurs in about 1 of every 40,000 births.".
- 18p- label "18p-".
- 18p- sameAs Q4557543.
- 18p- sameAs m.04gjd82.
- 18p- sameAs Q4557543.
- 18p- wasDerivedFrom 18p-?oldid=619074161.
- 18p- isPrimaryTopicOf 18p-.
- 18p- name "18p-".