omphalocele Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
Description	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. (Human Disease Ontology, DOID_0060327)
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Genes

13 genes co-occuring with the biological term omphalocele in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
ALX4	ALX homeobox 4
BMP1	bone morphogenetic protein 1
BMPR1A	bone morphogenetic protein receptor, type IA
CAT	catalase
CD320	CD320 molecule
GLI3	GLI family zinc finger 3
HOXB2	homeobox B2
HOXB4	homeobox B4
MSX1	msh homeobox 1
MSX2	msh homeobox 2
MTHFR	methylenetetrahydrofolate reductase (NAD(P)H)
SOD2	superoxide dismutase 2, mitochondrial
ZIC3	Zic family member 3