Catalog

Hereditary renal hypouricemia

No MMS code

Link to WHO Definition

Hereditary renal hypouricemia – http://id.who.int/icd/entity/479364233

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).