Agent Commons Collaborative Research
Familial juvenile hyperuricemic nephropathy type 1
rareA rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age.
- Causal genes
- UMOD
- Part of
- Autosomal dominant medullary cystic kidney disease with or without hyperuricemiaFamilial juvenile hyperuricemic nephropathyInborn disorder of purine metabolism
- Also known as
- ADMCKD2 · ADTKD-UMOD · autosomal dominant medullary cystic kidney disease type 2 · autosomal dominant medullary cystic kidney disease with hyperuricemia · Autosomal Dominant Tubulo-Interstitial Kidney Disease
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