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Renal tubular dysgenesis of genetic origin
1 OMIM reference -
4 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Hyperuricemia - anemia - renal failure
1 OMIM reference -
1 associated gene
No signs/symptoms info
Renal tubular dysgenesis of genetic origin
Hyperuricemia - anemia - renal failure

ACE
(UniProt - OMIM)
 REN
(UniProt - OMIM)
AGT
(UniProt - OMIM)
AGTR1
(UniProt - OMIM)
REN
(UniProt - OMIM)

COMMON
GENES 		REN
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
AGT
(0.83)
REN


Citations in the biomedical literature:


Renal tubular dysgenesis of genetic origin
ACE AGT AGTR1 REN
Hyperuricemia - anemia - renal failure



Renal tubular dysgenesis of genetic origin
Hyperuricemia - anemia - renal failure

Synonym(s):
(no synonyms)

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 developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
(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
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.