Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q3508565> ?p ?o }
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- Q3508565 subject Q6500135.
- Q3508565 subject Q6853484.
- Q3508565 subject Q7022834.
- Q3508565 subject Q7867720.
- Q3508565 abstract "ABCD syndrome is the acronym for albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness. It has been found to be caused by mutation in the endothelin B receptor gene (EDNRB).".
- Q3508565 omim "600501".
- Q3508565 thumbnail Patient_with_Waardenburg-Klein_syndrome_(1916).jpg?width=300.
- Q3508565 wikiPageExternalLink OMIM.
- Q3508565 wikiPageExternalLink carddisp?gene=EDNRB.
- Q3508565 wikiPageWikiLink Q101244.
- Q3508565 wikiPageWikiLink Q1151801.
- Q3508565 wikiPageWikiLink Q12133.
- Q3508565 wikiPageWikiLink Q13048280.
- Q3508565 wikiPageWikiLink Q1343645.
- Q3508565 wikiPageWikiLink Q1438099.
- Q3508565 wikiPageWikiLink Q169872.
- Q3508565 wikiPageWikiLink Q18023174.
- Q3508565 wikiPageWikiLink Q246809.
- Q3508565 wikiPageWikiLink Q247101.
- Q3508565 wikiPageWikiLink Q281289.
- Q3508565 wikiPageWikiLink Q344522.
- Q3508565 wikiPageWikiLink Q3705665.
- Q3508565 wikiPageWikiLink Q42918.
- Q3508565 wikiPageWikiLink Q43054.
- Q3508565 wikiPageWikiLink Q48255.
- Q3508565 wikiPageWikiLink Q592830.
- Q3508565 wikiPageWikiLink Q6500135.
- Q3508565 wikiPageWikiLink Q6853484.
- Q3508565 wikiPageWikiLink Q7022834.
- Q3508565 wikiPageWikiLink Q7430.
- Q3508565 wikiPageWikiLink Q7867720.
- Q3508565 wikiPageWikiLink Q8084905.
- Q3508565 wikiPageWikiLink Q81867.
- Q3508565 name "ABCD syndrome".
- Q3508565 omim "600501".
- Q3508565 type Disease.
- Q3508565 type Thing.
- Q3508565 type Q12136.
- Q3508565 comment "ABCD syndrome is the acronym for albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness. It has been found to be caused by mutation in the endothelin B receptor gene (EDNRB).".
- Q3508565 label "ABCD syndrome".
- Q3508565 depiction Patient_with_Waardenburg-Klein_syndrome_(1916).jpg.
- Q3508565 name "ABCD syndrome".