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Hyperuricemia - anemia - renal failure
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Renal tubular dysgenesis of genetic origin
X-linked intellectual disability, Hedera type
X-linked parkinsonism-spasticity syndrome
Obesity due to prohormone convertase I deficiency
Synonym(s):
- FJHN type 2
- Familial juvenile hyperuricemic nephropathy type 2
- REN-associated FJHN
- REN-associated familial juvenile hyperuricemic nephropathy
- REN-associated kidney disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
REN P00797179820
No signs/symptoms info available.