Acquired hyporeninemic hypoaldosteronism

Addison’s disease

Congenital adrenal hyperplasia (recesssive or autosomal dominant)

Mineralocorticoid deficiency

Primary hypoaldosteronism or hyporeninemia

Pseudohypoaldosteronism

Renal insufficiency or failure

Systemic lupus erythematosus

Type IV renal tubular acidosis

Acidosis

Damage to tissue from rhabdomyolysis, burns, or trauma

Familial hyperkalemic periodic paralysis

Hyperosmolar states, (e.g., uncontrolled diabetes, glucose infusions)

Insulin deficiency or resistance

Tumor lysis syndrome