visceral heterotaxy Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen. (Human Disease Ontology, DOID_0050545)
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Genes

7 genes involed in the disease visceral heterotaxy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ACVR2B activin A receptor, type IIB
CFC1 cripto, FRL-1, cryptic family 1
CFC1B cripto, FRL-1, cryptic family 1B
GALNT11 polypeptide N-acetylgalactosaminyltransferase 11
LEFTY2 left-right determination factor 2
NODAL nodal growth differentiation factor
ZIC3 Zic family member 3