Hereditary renal hypouricemia

MONDO:0009071

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).

Also known as: Dalmatian hypouricemia, hypouricemia, renal, renal hypouricemia

13 clinical trials for this condition and its sub-types.

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