"Monosomy 13q SyndromePTNICHD" . . "13q Deletion SyndromeSYNCI" . "C0265451"^^ . "NICHD"^^ . "A rare syndrome that is characterized by the partial deletion of the long arm of chromosome 13. Signs and symptoms include low birth weight, craniofacial malformations, hands and feet malformations, and mental and psychomotor retardation.NCI" . . . "Disease or Syndrome"^^ . "C98993"^^ . "Monosomy 13q Syndrome"^^ . . "Monosomy 13q Syndrome"^^ . "Monosomy 13q SyndromePTNCI" . .