hypercholanemia, familial Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/607748
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Genes

3 genes associated with the hypercholanemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
BAAT bile acid CoA:amino acid N-acyltransferase
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
TJP2 tight junction protein 2