Familial juvenile hyperuricemic nephropathy type 1

MONDO:0008073

A rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age.

Also known as: familial juvenile gouty nephropathy, familial nephropathy with gout, gouty nephropathy, familial juvenile, hyperuricemic nephropathy, familial juvenile, nephropathy, familial, with gout, ADTKD-UMOD, Autosomal Dominant Tubulo-Interstitial Kidney Disease, FJHN type 1

2 clinical trials for this condition and its sub-types, 0 tagged with Familial juvenile hyperuricemic nephropathy type 1 itself.

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↑ Inborn disorder of purine metabolism (14) ↑ Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (7) ↑ Familial juvenile hyperuricemic nephropathy (0)

Including sub-types (2) Tagged with Familial juvenile hyperuricemic nephropathy type 1 (0)

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