ABCD3 (ATP Binding Cassette Subfamily D Member 3) is a Protein Coding gene. Diseases associated with ABCD3 include Bile Acid Synthesis Defect, Congenital, 5 and Zellweger Syndrome. Among its related pathways are Nuclear Receptors in Lipid Metabolism and Toxicity and CDK-mediated phosphorylation and removal of Cdc6.