Also Known As
familial juvenile gouty nephropathyfamilial nephropathy with goutgouty nephropathy, familial juvenilehyperuricemic nephropathy, familial juvenilenephropathy, familial, with goutADTKD-UMODAutosomal Dominant Tubulo-Interstitial Kidney DiseaseFJHN type 1HNFJ1UMOD familial juvenile hyperuricemic nephropathyUMOD-associated FJHNUMOD-associated familial juvenile hyperuricemic nephropathyUMOD-related ADTKDUMOD-related kidney diseaseautosomal dominant medullary cystic kidney disease type 2autosomal dominant medullary cystic kidney disease with hyperuricemiaautosomal dominant tubulointerstitial kidney disease - UMODautosomal dominant tubulointerstitial kidney disease due to mutations in UMODfamilial juvenile hyperuricemic nephropathy caused by mutation in UMODglomerulocystic kidney disease with hyperuricemia and isosthenuriahyperuricemic nephropathy, familial juvenile, 1hyperuricemic nephropathy, familial juvenile, type 1medullary cystic kidney disease 2medullary cystic kidney disease type 2medullary cystic kidney disease type IItubulointerstitial kidney disease, autosomal dominant, 1uromodulin storage diseaseuromodulin-associated kidney diseaseADMCKD2MCKD2UMOD-related autosomal dominant tubulointerstitial kidney diseasefamilial juvenile hyperuricaemic nephropathymedullary cystic kidney disease 2, autosomal dominant
Definition
A rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age.