Catel-Manzke syndrome
ORPHA:1388Non-syndromic polydactyly, syndactyly and/or hyperphalangy
ORPHA:93458OBSOLETE: Syndrome associated with Pierre Robin syndrome
ORPHA:138063Pierre Robin syndrome-faciodigital anomaly syndrome
ORPHA:2888Robin sequence-oligodactyly syndrome
ORPHA:3104TARP syndrome
ORPHA:2886Weissenbacher-Zweymuller syndrome
ORPHA:3450