Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q2691713> ?p ?o }
Showing triples 1 to 46 of
46
with 100 triples per page.
- Q2691713 subject Q6500135.
- Q2691713 subject Q8543557.
- Q2691713 abstract "Miller syndrome is a genetic condition also known as the Genee-Wiedemann syndrome, Wildervanck-Smith syndrome, or postaxial acrofacial dystosis. The incidence of this condition is not known, but it is considered extremely rare. It is due to a mutation in the DHODH gene. Nothing is known of its pathogenesis.".
- Q2691713 omim "263750".
- Q2691713 wikiPageWikiLink Q1072.
- Q2691713 wikiPageWikiLink Q1100988.
- Q2691713 wikiPageWikiLink Q1150909.
- Q2691713 wikiPageWikiLink Q12811075.
- Q2691713 wikiPageWikiLink Q130888.
- Q2691713 wikiPageWikiLink Q1462309.
- Q2691713 wikiPageWikiLink Q166231.
- Q2691713 wikiPageWikiLink Q172605.
- Q2691713 wikiPageWikiLink Q176503.
- Q2691713 wikiPageWikiLink Q180323.
- Q2691713 wikiPageWikiLink Q188641.
- Q2691713 wikiPageWikiLink Q196672.
- Q2691713 wikiPageWikiLink Q2072063.
- Q2691713 wikiPageWikiLink Q207722.
- Q2691713 wikiPageWikiLink Q220815.
- Q2691713 wikiPageWikiLink Q222634.
- Q2691713 wikiPageWikiLink Q2823223.
- Q2691713 wikiPageWikiLink Q321285.
- Q2691713 wikiPageWikiLink Q372016.
- Q2691713 wikiPageWikiLink Q39572.
- Q2691713 wikiPageWikiLink Q425536.
- Q2691713 wikiPageWikiLink Q48228.
- Q2691713 wikiPageWikiLink Q507032.
- Q2691713 wikiPageWikiLink Q531029.
- Q2691713 wikiPageWikiLink Q6500135.
- Q2691713 wikiPageWikiLink Q7107685.
- Q2691713 wikiPageWikiLink Q7362.
- Q2691713 wikiPageWikiLink Q744790.
- Q2691713 wikiPageWikiLink Q7886.
- Q2691713 wikiPageWikiLink Q8047.
- Q2691713 wikiPageWikiLink Q838139.
- Q2691713 wikiPageWikiLink Q8543557.
- Q2691713 wikiPageWikiLink Q9614.
- Q2691713 wikiPageWikiLink Q9655.
- Q2691713 name "Miller syndrome".
- Q2691713 omim "#263750".
- Q2691713 type Disease.
- Q2691713 type Thing.
- Q2691713 type Q12136.
- Q2691713 comment "Miller syndrome is a genetic condition also known as the Genee-Wiedemann syndrome, Wildervanck-Smith syndrome, or postaxial acrofacial dystosis. The incidence of this condition is not known, but it is considered extremely rare. It is due to a mutation in the DHODH gene. Nothing is known of its pathogenesis.".
- Q2691713 label "Miller syndrome".
- Q2691713 name "Miller syndrome".