DISEASES

Disease-gene associations mined from literature

Human genes for omphalocele

Omphalocele [DOID:0060327]

A physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac.

Synonyms:  omphalocele,  DOID:0060327,  omphaloceles,  omphalocoele,  omphalocoeles