congenital megacolon; hirschsprung disease; urea cycle disorders, inborn Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group developmental (Genetic Association Database)
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Genes

3 genes associated with the disease congenital megacolon; hirschsprung disease; urea cycle disorders, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
RET ret proto-oncogene
SVEP1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1