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Familial juvenile hyperuricemic nephropathy type 1
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Synonym(s):
- FJHN type 1
- Familial juvenile gouty nephropathy
- Familial nephropathy with gout
- UMOD-associated FJHN
- UMOD-associated familial juvenile hyperuricemic nephropathy
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
UMOD P07911191845
No signs/symptoms info available.