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Juvenile gout [Supplementary Concept]

An autosomal dominant disorder characterized by hyperuricemia due to a low fractional excretion of URIC ACID, defective urinary concentrating ability, interstitial nephropathy, and progression to CHRONIC KIDNEY FAILURE. Both HNFJ1 and medullary cystic kidney disease (MCKD2) (OMIM: 603860) are caused by mutations in the UMOD gene. OMIM: 162000

Date introduced: August 25, 2010

MeSH Unique ID: C537696

Heading Mapped to:

Entry Terms:

  • HNFJ
  • Gouty nephropathy, familial juvenile
  • Nephropathy, familial, with gout
  • Hyperuricemic Nephropathy, Familial Juvenile 1
  • Familial Juvenile Hyperuricemic Nephropathy
  • Hyperuricemic Nephropathy, Familial Juvenile
  • Uromodulin-Associated Kidney Disease
  • Familial Gout-Kidney Disease
  • Familial Gouty Nephropathy
  • Mckd2
  • Medullary Cystic Kidney Disease Type 2
  • Umod-Related Kidney Disease
  • HNFJ1
  • Uromodulin Storage Disease

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