pseudohypoaldosteronism type 2 NANDO:2200369 OMIMPS:145260 NCIT:C123252 Spitzer-Weinstein syndrome SCTID:15689008 Orphanet:757 PHA2 PHAII MEDGEN:259599 Gordon syndrome familial hyperkalemic hypertension Gordon hyperkalemia-hypertension syndrome hyperpotassemia and hypertension familial GARD:0004553 pseudohypoaldosteronism, type II UMLS:C1449844 MONDO:0019162 chloride shunt syndrome hypertensive hyperkalemia pseudohypoaldosteronism, type 2 mineralocorticoid resistant hyperkalemia A rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function. ICD9:588.89 icd11.foundation:715347509 hyperkalemia-hypertension syndrome, Gordon type inherited pseudohypoaldosteronism