A rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function. The disease is pseudohypoaldosteronism type 2 (MONDO_0019162). Also known as: Gordon hyperkalemia-hypertension syndrome, PHA2, PHAII, Spitzer-Weinstein syndrome, chloride shunt syndrome, familial hyperkalemic hypertension, hyperkalemia-hypertension syndrome, Gordon type, hypertensive hyperkalemia.