hyperuricaemic nephropathy, familial juvenile 1
hyperuricaemic nephropathy, familial juvenile 1
An autosomal dominant renal disorder (OMIM:162000) characterised by juvenile onset of hyperuricaemia, polyuria, progressive renal failure, gout and fibrosis of the renal interstitium.Molecular pathology
Caused by defects of UMOD, which encodes uromodulin, the most abundant protein in urine.