ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

1 OMIM reference -
4 associated genes
No signs/symptoms info

Hyperuricemia - anemia - renal failure

Renal tubular dysgenesis of genetic origin


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

Citations in the biomedical literature:

Hyperuricemia - anemia - renal failure		Renal tubular dysgenesis of genetic origin
	Synonym(s): - FJHN type 2 - Familial juvenile hyperuricemic nephropathy type 2 - REN-associated FJHN - REN-associated familial juvenile hyperuricemic nephropathy - REN-associated kidney disease		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare renal disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.