hereditary renal hypouricemia Dalmatian hypouricemia GARD:0009496 Hereditary renal hypouricemia (HRH) is a rare autosomal recessively inherited renal membrane transport disorder affecting urate reabsorption in the proximal tubules leading to usually asymptomatic hypouricemia and predisposing to urolithiasis and exercise induced acute renal failure (EIARF). ICD9:790.6 MESH:C537757 MONDO:0009071 Orphanet:94088 SCTID:236478009 hypouricemia, renal renal hypouricemia inherited renal tubular disease rare renal tubular disease