{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/143890
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Genes

1 genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
EPHX2 epoxide hydrolase 2, cytoplasmic