OBSOLETE: Syndrome associated with Pierre Robin syndrome
ORPHA:138063Catel-Manzke syndrome
ORPHA:1388Isolated Pierre Robin sequence
ORPHA:718OBSOLETE: ATR-X-related syndrome
ORPHA:263355OBSOLETE: Dysmorphic syndrome associated with bone anomaly
ORPHA:93472OBSOLETE: Ectodermal malformation syndrome associated with ocular features
ORPHA:98709OBSOLETE: Pierre Robin syndrome associated with miscellaneous anomalies
ORPHA:138066OBSOLETE: Sequence or association
ORPHA:139006OBSOLETE: Sucking/swallowing disorder associated with an identified syndrome
ORPHA:138072OBSOLETE: Sucking/swallowing disorder not related with Pierre Robin syndrome
ORPHA:138069OBSOLETE: Syndrome associated with a congenital cardiopathy
ORPHA:98732OBSOLETE: Syndromic ichthyosis associated with ocular features
ORPHA:98699Pierre Robin syndrome associated with a chromosomal anomaly
ORPHA:138047Pierre Robin syndrome associated with bone disease
ORPHA:138055Pierre Robin syndrome associated with branchial archs anomalies
ORPHA:138050Pierre Robin syndrome associated with collagen disease
ORPHA:138041Pierre Robin syndrome-faciodigital anomaly syndrome
ORPHA:2888Rare disease with Pierre Robin syndrome
ORPHA:138044Robin sequence-oligodactyly syndrome
ORPHA:3104Weissenbacher-Zweymuller syndrome
ORPHA:3450