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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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