Agent Commons Collaborative Research
Hereditary renal hypouricemia
rareHereditary 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).
- Identifiers
- MONDO:0009071 Orphanet:94088
- Part of
- Inherited renal tubular disease
- Also known as
- hypouricemia, renal
Subtypes
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