Familial omphalocele syndrome with facial dysmorphism

Parents (6)

• 11164009Autosomal dominant hereditary disorder disorder
• 126764002Congenital anomaly of intestinal tract disorder
• 18735004Congenital omphalocele disorder
• 363070008Developmental hereditary disorder disorder
• 363080007Digestive system hereditary disorder disorder
• 65094009Multiple malformation syndrome with facial defects as major feature disorder

Children (0)

None (leaf concept).