familial juvenile hyperuricemic nephropathy

Findings

No curated finding names familial juvenile hyperuricemic nephropathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, hp/releases/2026-09-01.

Where it sits

A kind of

• inherited kidney disorder

Narrower terms (6)

• familial juvenile hyperuricemic nephropathy type 1
• familial juvenile hyperuricemic nephropathy type 2
• hyperuricemic nephropathy, familial juvenile type 3
• hyperuricemic nephropathy, familial juvenile type 4
• tubulointerstitial kidney disease, autosomal dominant 6
• tubulointerstitial kidney disease, autosomal dominant, 2

Resolves to: familial juvenile hyperuricemic nephropathy

Also called

familial juvenile gouty nephropathyfamilial nephropathy associated with hyperuricemiafamilial nephropathy with goutFJHNgouty nephropathy, familial juvenilejuvenile goutjuvenile gouty nephropathynephropathy, familial, with gouttubulointerstitial kidney disease