Hereditary renal hypouricemia
ORPHA:94088· ICD-10 N25.8
Definition
A genetic renal tubular disorder characterized by urinary urate wasting that typically leads to asymptomatic hypouricemia and predisposes to urolithiasis and exercise-induced acute renal failure (EIARF).
- Prevalence
- Unknown
- Inheritance
- Autosomal recessive
- Age of onset
- All ages