Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q525642> ?p ?o }
- Q525642 wikiPageWikiLink Q7129609.
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- Q525642 icd ",".
- Q525642 icd "279.11".
- Q525642 icd "758.32".
- Q525642 icd "D82.1".
- Q525642 name "22".
- Q525642 omim "188400".
- Q525642 type Disease.
- Q525642 type Thing.
- Q525642 type Q12136.
- Q525642 comment "DiGeorge syndrome is also known as 22q11.2 deletion syndrome,DiGeorge anomaly, velocardiofacial syndrome (VCFS), Shprintzen syndrome, conotruncal anomaly face syndrome (CTAF) or Takao syndrome, Sedlackova syndrome, Cayler cardiofacial syndrome,Strong syndrome, congenital thymic aplasia, and thymic hypoplasia. This syndrome is caused by the deletion of a small piece of chromosome 22.".
- Q525642 label "DiGeorge syndrome".
- Q525642 depiction Brain_computer_tomography_cuts_of_the_patient_with_22q11.2_syndrome,_demonstrating_basal_ganglia_and_periventricular_calcification.jpg.
- Q525642 name "22q11.2 deletion syndrome".