Disease Summary help help Associated Targets (1)Tbio1 Explore Associated Targets list GARD Rare open_in_new Mondo Description Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. Mondo Term and Equivalent IDs MONDO:0009869: isolated Pierre-Robin syndrome GARD:0004347: open_in_newGARD:0004354: open_in_newMESH:D010855: open_in_newNCIT:C85010: open_in_newOMIM:261800: PIERRE ROBIN SYNDROMEopen_in_newOrphanet:718: SCTID:4602007: open_in_new