disease has feature Pierre-Robin sequence syndromic disease eye disorder isolated Pierre-Robin syndrome https://github.com/monarch-initiative/mondo/issues/9147 https://www.malacards.org/card/pierre_robin_syndrome SCTID:4602007 Orphanet:718 MESH:D010855 NCIT:C85010 Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. OMIM:261800 UMLS:C0031900 GARD:0004347 MONDO:0009869 Pierre Robin Sequence isolated Pierre Robin sequence NORD:1579 glossoptosis, micrognathia, and cleft palate Pierre Robin syndrome skeletal dysplasia polydactyly MEDGEN:19310 icd11.foundation:136361299 obsolete syndrome or malformation associated with head and neck malformations