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Familial juvenile hyperuricemic nephropathy type 1

Orpha number ORPHA209886
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 Variable
ICD-10 -
OMIM
UMLS -
MeSH -
MedDRA -
SNOMED CT -

Summary

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


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Detailed information

Clinical genetics review
  • EN (2013)
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