ABCC8 (ATP Binding Cassette Subfamily C Member 8) is a Protein Coding gene. Diseases associated with ABCC8 include Hyperinsulinemic Hypoglycemia, Familial, 1 and Hypoglycemia Of Infancy, Leucine-Sensitive. Among its related pathways are Type II diabetes mellitus and CDK-mediated phosphorylation and removal of Cdc6.