ODCs

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

PROTEIN INTERACTIONS: 1

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

Hyperuricemia - anemia - renal failure

X-linked parkinsonism-spasticity syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	REN	(0.78)	ATP6AP2

Citations in the biomedical literature:

Hyperuricemia - anemia - renal failure		X-linked parkinsonism-spasticity syndrome
	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): - XPDS

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		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		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: x-linked recessive

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

No signs/symptoms info available.