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- Q1756040 subject Q6500135.
- Q1756040 subject Q6907472.
- Q1756040 abstract "Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation, Pierre Robin anomaly or Pierre Robin anomalad) is a congenital condition of facial abnormalities in humans. PRS is a sequence, i.e. a chain of certain developmental malformations, one entailing the next. The three main features are cleft palate, retrognathia (abnormal positioning of the jaw or maxilla) and glossoptosis (airway obstruction caused by backwards displacement of the tongue base). A genetic cause to PRS was recently identified. Pierre Robin sequence may be caused by genetic anomalies at chromosomes 2, 11, or 17.".
- Q1756040 icd10 "Q87.0".
- Q1756040 icd9 "756.0".
- Q1756040 meshId "D010855".
- Q1756040 omim "261800".
- Q1756040 wikiPageExternalLink OC_Exp.php?Lng=GB&Expert=718.
- Q1756040 wikiPageExternalLink ?aModele=afficheN&cpsidt=18787770.
- Q1756040 wikiPageExternalLink mainpageS1894P0.html.
- Q1756040 wikiPageExternalLink www.pierrerobin.com.
- Q1756040 wikiPageExternalLink www.pierrerobin.org.
- Q1756040 wikiPageExternalLink http://www.seattlechildrens.org/medical-conditions/chromosomal-genetic-conditions/pierre/#.
- Q1756040 wikiPageExternalLink www.tremplin-spr.org.
- Q1756040 wikiPageWikiLink Q105688.
- Q1756040 wikiPageWikiLink Q1100988.
- Q1756040 wikiPageWikiLink Q1566784.
- Q1756040 wikiPageWikiLink Q17002116.
- Q1756040 wikiPageWikiLink Q172605.
- Q1756040 wikiPageWikiLink Q179630.
- Q1756040 wikiPageWikiLink Q189553.
- Q1756040 wikiPageWikiLink Q1901516.
- Q1756040 wikiPageWikiLink Q2125439.
- Q1756040 wikiPageWikiLink Q222634.
- Q1756040 wikiPageWikiLink Q223591.
- Q1756040 wikiPageWikiLink Q2288646.
- Q1756040 wikiPageWikiLink Q2559234.
- Q1756040 wikiPageWikiLink Q2575857.
- Q1756040 wikiPageWikiLink Q281078.
- Q1756040 wikiPageWikiLink Q284219.
- Q1756040 wikiPageWikiLink Q324921.
- Q1756040 wikiPageWikiLink Q3267428.
- Q1756040 wikiPageWikiLink Q4330029.
- Q1756040 wikiPageWikiLink Q504033.
- Q1756040 wikiPageWikiLink Q525642.
- Q1756040 wikiPageWikiLink Q5283631.
- Q1756040 wikiPageWikiLink Q5571959.
- Q1756040 wikiPageWikiLink Q6500135.
- Q1756040 wikiPageWikiLink Q6907472.
- Q1756040 wikiPageWikiLink Q7192427.
- Q1756040 wikiPageWikiLink Q744790.
- Q1756040 wikiPageWikiLink Q7452454.
- Q1756040 wikiPageWikiLink Q939018.
- Q1756040 wikiPageWikiLink Q9614.
- Q1756040 icd "756".
- Q1756040 icd "Q87.0".
- Q1756040 meshid "D010855".
- Q1756040 name "Pierre Robin Sequence".
- Q1756040 omim "261800".
- Q1756040 type Disease.
- Q1756040 type Thing.
- Q1756040 type Q12136.
- Q1756040 comment "Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation, Pierre Robin anomaly or Pierre Robin anomalad) is a congenital condition of facial abnormalities in humans. PRS is a sequence, i.e. a chain of certain developmental malformations, one entailing the next. The three main features are cleft palate, retrognathia (abnormal positioning of the jaw or maxilla) and glossoptosis (airway obstruction caused by backwards displacement of the tongue base).".
- Q1756040 label "Pierre Robin syndrome".
- Q1756040 name "Pierre Robin Sequence".