genetic hypertension pseudohypoaldosteronism pseudohypoaldosteronism type 2 GARD:0004553 Gordon hyperkalemia-hypertension syndrome Gordon syndrome ICD10:I15.1 ICD9:588.89 MONDO:0019162 NCIT:C123252 OMIMPS:145260 Orphanet:757 PHA2 PHAII Pseudohypoaldosteronism type 2 (PHA2) is a rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function. SCTID:15689008 Spitzer-Weinstein syndrome UMLS:C1449844 chloride shunt syndrome familial hyperkalemic hypertension hyperkalemia-hypertension syndrome, Gordon type hyperpotassemia and hypertension familial hypertensive hyperkalemia mineralocorticoid resistant hyperkalemia pseudohypoaldosteronism, type 2 pseudohypoaldosteronism, type II