bile acid malabsorption, primary Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/613291
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Genes

1 genes associated with the bile acid malabsorption, primary phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2