cerebrotendinous xanthomatosis Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A xanthomatosis that is characterized by a deficiency in the production of the bile acid, chenodeoxycholic acid that has_material_basis_in autosomal recessive inheritance and results in cholestanol deposition in the brain and other tissues and with elevated levels of cholesterol in plasma. (Human Disease Ontology, DOID_4810)
External Link http://www.omim.org/entry/213700
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Genes

1 genes associated with the cerebrotendinous xanthomatosis phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1