These disease states include primary aldosteronism (PA), as well as conditions that manifest with low aldosterone levels, such as endogenous hypercortisolism, the syndrome of apparent mineralocorticoid excess (AME), atypical forms of congenital adrenal hyperplasia, and alterations in the activity of the mineralocorticoid receptor or epithelial sodium channel (Liddle syndrome). This evidence concerns the gene NR3C2 and congenital adrenal hyperplasia.