ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Xanthinuria type II

Familial renal amyloidosis due to Apolipoprotein AI variant


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MOCOS	(0.72)	APOA1

Citations in the biomedical literature:

Xanthinuria type II		Familial renal amyloidosis due to Apolipoprotein AI variant
	Synonym(s): - XDH and AOX dual deficiency - Xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency		Synonym(s): - Apolipoprotein AI amyloidosis - Familial amyloid nephropathy due to apolipoprotein AI variant - Hereditary amyloid nephropathy due to apolipoprotein AI variant - Hereditary renal amyloidosis due to apolipoprotein AI variant

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

No signs/symptoms info available.