Shprintzen Goldberg omphalocele syndrome

Shprintzen Goldberg omphalocele syndrome (disorder)

active

Code	`716230005`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20160731

Synonyms

Omphalocele syndrome Shprintzen Goldberg type

Parents (4)

11164009Autosomal dominant hereditary disorder disorder
18735004Congenital omphalocele disorder
363070008Developmental hereditary disorder disorder
65094009Multiple malformation syndrome with facial defects as major feature disorder

Children (0)

None (leaf concept).