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Familial juvenile hyperuricemic nephropathy type 1

Disease definition

Familial juvenile hyperuricemic nephropathy type 1 (FJHN1) is a rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age.

ORPHA:209886

  • Synonym(s):
    • FJHN type 1
    • Familial juvenile gouty nephropathy
    • Familial nephropathy with gout
    • UMOD-associated FJHN
    • UMOD-associated familial juvenile hyperuricemic nephropathy
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: All ages
  • ICD-10: -
  • OMIM: 162000
  • UMLS: -
  • MeSH: -
  • GARD: 6806
  • MedDRA: -

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