hereditary renal hypouricemia https://www.malacards.org/card/hereditary_renal_hypouricemia MONDO:0009071 icd11.foundation:479364233 SCTID:236478009 GARD:0009496 MESH:C537757 Orphanet:94088 ICD9:790.6 UMLS:C4551590 MEDGEN:1643078 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). hypouricemia, renal inherited renal tubular disease