Catel-Manzke syndrome
ORPHA:1388Genetic syndromic Pierre Robin syndrome
ORPHA:363294Pierre Robin syndrome associated with a chromosomal anomaly
ORPHA:138047Pierre Robin syndrome associated with branchial archs anomalies
ORPHA:138050Pierre Robin syndrome-faciodigital anomaly syndrome
ORPHA:2888Rare disease with Pierre Robin syndrome
ORPHA:138044Robin sequence-oligodactyly syndrome
ORPHA:3104Teratogenic Pierre Robin syndrome
ORPHA:138059Weissenbacher-Zweymuller syndrome
ORPHA:3450