ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Dense deposit disease

Familial renal amyloidosis due to Apolipoprotein AI variant

CFH	(UniProt - OMIM)		APOA1	(UniProt - OMIM)
CFHR1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CFHR1	(0.62)	APOA1

Citations in the biomedical literature:

Dense deposit disease		Familial renal amyloidosis due to Apolipoprotein AI variant
	Synonym(s): - Membranoproliferative glomerulonephritis type 2		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): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: D015432		External references: No OMIM references No MeSH references

No signs/symptoms info available.