ABCG8 and hyperinsulinemic hypoglycemia, familial, 4: Reynolds syndrome (4), Combined hyperlipidemia, familial (2), Congenital generalized lipodystrophy type 2 (1), Sitosterolemia due to ABCG8 deficiency (1), Hyperalphalipoproteinemia (1), Hypobetalipoproteinemia (1)