Xanthomatosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A lipid storage disease that is characterized by the desposition of yellowish cholesterol-rich material in tendons or other body parts. (Human Disease Ontology, DOID_3345)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014973
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Genes

1 genes/proteins associated with the disease Xanthomatosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5 2.88009